Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexU.S. General Services Administration, National Archives and Records Service, Office of the Federal Register, 1990 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 66.
vi. lappuse
... listed in the Finding Aids at the end of this volume . What if the material incorporated by reference cannot be found ? If you have any problem locating or obtaining a copy of material listed in the Finding Aids of this volume as an ...
... listed in the Finding Aids at the end of this volume . What if the material incorporated by reference cannot be found ? If you have any problem locating or obtaining a copy of material listed in the Finding Aids of this volume as an ...
3. lappuse
... listing for manufacturers of devices ........ 46 808 Exemptions from Federal preemption of State and local medical device requirements ........... 58 809 812 In vitro diagnostic products for human use Investigational device exemptions ...
... listing for manufacturers of devices ........ 46 808 Exemptions from Federal preemption of State and local medical device requirements ........... 58 809 812 In vitro diagnostic products for human use Investigational device exemptions ...
7. lappuse
... listed below except to the extent that a product's manufacturer or packer has obtained an exemption from a packaging or la- beling requirement : ( 1 ) Initial effective date for packag- ing requirements . ( i ) The packaging requirement ...
... listed below except to the extent that a product's manufacturer or packer has obtained an exemption from a packaging or la- beling requirement : ( 1 ) Initial effective date for packag- ing requirements . ( i ) The packaging requirement ...
9. lappuse
... listed in § 5.115 of this chapter ) who is permitted by § 16.42 ( a ) of this chapter to preside over the hearing . ( 5 ) If the appellant requests a regu- latory hearing and requests that the hearing be held within 5 working days after ...
... listed in § 5.115 of this chapter ) who is permitted by § 16.42 ( a ) of this chapter to preside over the hearing . ( 5 ) If the appellant requests a regu- latory hearing and requests that the hearing be held within 5 working days after ...
31. lappuse
... listed in any order of frequency or severity . Reported adverse reactions include : endo- metritis , spontaneous abortion , septic abor- tion , septicemia , perforation of the uterus and cervix , embedment , fragmentation of the IUD ...
... listed in any order of frequency or severity . Reported adverse reactions include : endo- metritis , spontaneous abortion , septic abor- tion , septicemia , perforation of the uterus and cervix , embedment , fragmentation of the IUD ...
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accessories amended at 53 ance standards application blood bone cement Cardiopulmonary bypass catheter cation chapter Class II perform Class III premar Classification clinical clude commercially distributed Commissioner complaint files component contact lens controls Date PMA denture device includes device intended device is exempt device that consists disease Drug Administration effective date emission equipment Federal Food fluid Food and Drug Health hearing aid Identification immunological test system implanted intended for medical intended to measure intraocular lens investigational study June 12 ket approval labeling laser laser product lens manufacturing practice means medical device medical purposes ment for premarket monitor notice of completion package paragraph patient PDP is required plasma PMA or notice premarket approval premarket notification procedures procedures in Subpart prosthesis radiation respect to complaint section 515 Sept serological serum sponsor statement submit surgical tion tissue tube type of device x-ray system
Populāri fragmenti
518. 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.
17. lappuse - Act upon removal from such processing, labeling, or repacking establishment. (b) (1) A drug intended for use by man which — (A) is a habit-forming drug to which section 502 (d) applies; or (B) because of its toxicity or other potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use, is not safe for use except under the supervision of a practitioner licensed by law to administer such drug...
528. lappuse - HHS of Customs for its release and delivery to the importer; but if, upon such final re-examination by such board, the tea shall be found to be inferior in purity, quality, and fitness for consumption, as compared with the said standards, the importer or consignee shall...
12. 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).
519. lappuse - Cream is that portion of milk, rich in milk fat, which rises to the surface of milk on standing, or is separated from it by centrifugal force, is fresh and clean and contains not less than eighteen (18) per cent of milk fat.
47. 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...
13. 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...
20. 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.
518. 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.
311. lappuse - ... (d) References in this part to regulatory sections of the Code of Federal Regulations are to Chapter I of Title 21 unless otherwise noted.