Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexDivision of the Federal Register, the National Archives, 1993 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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1.–5. rezultāts no 99.
vi. lappuse
... submitted for publication in accordance with 1 CFR part 51 . Properly approved incorporations by reference in this volume are listed in the Finding Aids at the end of this volume . What if the material incorporated by reference cannot ...
... submitted for publication in accordance with 1 CFR part 51 . Properly approved incorporations by reference in this volume are listed in the Finding Aids at the end of this volume . What if the material incorporated by reference cannot ...
6. lappuse
... submitted in the form of a citi- zen petition under § 10.30 of this chap- ter and should be clearly identified on the envelope as a “ Request for Exemp- tion from Tamper - resistant Rule . " A petition for an exemption from a re ...
... submitted in the form of a citi- zen petition under § 10.30 of this chap- ter and should be clearly identified on the envelope as a “ Request for Exemp- tion from Tamper - resistant Rule . " A petition for an exemption from a re ...
41. lappuse
... submitted in accordance with the re- quirements of § 10.30 of this chapter , demonstrating that the alternative test method will yield results that are equivalent to the results yielded by the test method specified in this sec- tion ...
... submitted in accordance with the re- quirements of § 10.30 of this chapter , demonstrating that the alternative test method will yield results that are equivalent to the results yielded by the test method specified in this sec- tion ...
43. lappuse
... submitted to FDA within 15 working days of initial receipt of the informa- tion . ( 2 ) Whenever a manufacturer or im- porter receives or otherwise becomes aware of information that reasonably suggests that one of its marketed de- vices ...
... submitted to FDA within 15 working days of initial receipt of the informa- tion . ( 2 ) Whenever a manufacturer or im- porter receives or otherwise becomes aware of information that reasonably suggests that one of its marketed de- vices ...
44. lappuse
... submitting the information to the manufacturer or importer ; ( 6 ) State whether the manufacturer or importer intends to submit addi- tional information , and , if so , when such information will be submitted ; and ( 7 ) State whether ...
... submitting the information to the manufacturer or importer ; ( 6 ) State whether the manufacturer or importer intends to submit addi- tional information , and , if so , when such information will be submitted ; and ( 7 ) State whether ...
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AC-powered accessories amended at 54 ance standards application blood bone cement Cardiopulmonary bypass catheter chapter Class II perform Class III premar Classification clinical clude commercially distributed Commissioner complaint files component controls current good manufacturing Date PMA denture device includes device intended device is exempt device that consists disease Drug Administration Effective date added equipment Federal Acquisition Regulation Federal Food Food and Drug Health hearing aid human Identification immunological test system implanted intended for medical intended to measure intraocular lens June 12 ket approval labeling laser laser product lens manufacturing practice medical purposes ment for premarket monitor National notice of completion Office operation paragraph patient PDP is required plasma PMA or notice premarket approval premarket notification procedures procedures in Subpart radiation respect to complaint revised section 515 Sept serological serum Service specific sponsor submitted surgical tion tissue tube type of device x-ray system
Populāri fragmenti
506. lappuse - Milk is the whole, fresh, clean, lacteal secretion obtained by the complete milking of one or more healthy cows, properly fed and kept, excluding that obtained •within 15 days before and 5 days after calving, or such longer period as may be necessary to render the milk practically colostrum free.
20. lappuse - Subpart D — Exemptions From Adequate Directions for Use § 801.109 Prescription devices. A device which, because of any potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use is not safe except under the supervision of a practitioner licensed by law to direct the use of such device, and hence for which "adequate directions for use...
516. lappuse - ... for its release and delivery to the importer; but if upon such final reexamination by such board the tea shall be found to be inferior in purity, quality, and fitness for consumption...
14. lappuse - The requirement for inclusion of the ZIP Code shall apply only to consumer commodity labels developed or revised after the effective date of this section. In the case of nonconsumer packages, the ZIP Code shall appear on either the label or the labeling (including the invoice).
49. lappuse - (1) the term 'manufacture, preparation, propagation, compounding, or processing' shall include repackaging or otherwise changing the container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place of manufacture to the person who makes final delivery or sale to the ultimate consumer; "(2) the term 'name...
22. lappuse - An exemption of a shipment or other delivery of a cosmetic under paragraph (a) (2) of this section shall become void ab initio with respect to the person who introduced such shipment or delivery into interstate commerce upon refusal by such person to make available for inspection a copy of the agreement, as required by such clause.
16. lappuse - Rico or in a Territory where the predominant language is one other than English, the predominant language may be substituted for English. (2) If the label contains any representation in a foreign language, all words, statements, and other information required by or under authority of the act to appear on the label shall appear thereon in the foreign language. (3) If the labeling contains any representation in a foreign language, all words, statements, and other information required by or under authority...
16. lappuse - No exemption depending on insufficiency of label space, as prescribed in regulations promulgated under section 502(b) of the act, shall apply if such insufficiency is caused by: (1) The use of label space for any word, statement, design, or device which is not required by or under authority of the act to appear on the label; (2) The use of label space to give greater conspicuousness to any word, statement, or other information than is required by section 502(c) of the act; or (3) The use of label...
506. lappuse - To regulate the Importation of milk and cream into the United States for the purpose of promoting the dairy industry of the United States and protecting the public health" shall be known and referred to as "the Federal Import Milk Act.
19. lappuse - On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any re-mainder in terms of ounces or common or decimal fractions of the pound...