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, 1996 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
No grāmatas satura
1.5. rezultāts no 100.
11. lappuse
... notice under §16.22 ( a ) of this chap- ter , provides notice of opportunity for a hearing under this section and is part of the administrative record of the reg- ulatory hearing under §16.80 ( a ) of this chapter . ( ii ) A request for ...
... notice under §16.22 ( a ) of this chap- ter , provides notice of opportunity for a hearing under this section and is part of the administrative record of the reg- ulatory hearing under §16.80 ( a ) of this chapter . ( ii ) A request for ...
28. lappuse
... notice for prospective hear- ing aid users required by paragraph ( c ) ( 3 ) of this section . ( xiii ) The technical data required by paragraph ( c ) ( 4 ) of this section , unless such data is provided in separate label- ing ...
... notice for prospective hear- ing aid users required by paragraph ( c ) ( 3 ) of this section . ( xiii ) The technical data required by paragraph ( c ) ( 4 ) of this section , unless such data is provided in separate label- ing ...
29. lappuse
... notice : IMPORTANT NOTICE FOR PROSPECTIVE HEARING AID USERS Good health practice requires that a per- son with a hearing loss have a medical eval- uation by a licensed physician ( preferably a physician who specializes in diseases of ...
... notice : IMPORTANT NOTICE FOR PROSPECTIVE HEARING AID USERS Good health practice requires that a per- son with a hearing loss have a medical eval- uation by a licensed physician ( preferably a physician who specializes in diseases of ...
87. lappuse
... notice of opportunity to request an oral hearing before the Commissioner or the Commissioner's designee . ( d ) A request for an oral hearing may be made by the State or political sub- division or any other interested person . Such ...
... notice of opportunity to request an oral hearing before the Commissioner or the Commissioner's designee . ( d ) A request for an oral hearing may be made by the State or political sub- division or any other interested person . Such ...
105. lappuse
... Notice of disapproval or withdrawal . If FDA disapproves an application or proposes to withdraw approval of an application , FDA will notify the spon- sor in writing . ( 1 ) A disapproval order will contain a complete statement of the ...
... Notice of disapproval or withdrawal . If FDA disapproves an application or proposes to withdraw approval of an application , FDA will notify the spon- sor in writing . ( 1 ) A disapproval order will contain a complete statement of the ...
Citi izdevumi - Skatīt visu
Bieži izmantoti vārdi un frāzes
acid amended at 54 ance standards antibodies application cardiopulmonary bypass catheter chapter Class II perform Class III premarket Classification cluding commercial distribution Commissioner complaint files Date PMA denture device intended device is exempt device that consists diagnosis and treatment distributor Drug Administration effective date established Federal Food Food and Drug hearing aid hemoglobin immunological test system implanted intended to measure intraocular lens inves investigational study June 12 labeling lens manufacturing practice medical device ment monitor notice of completion pacemaker package panel paragraph patient PDP is required petition plasma PMA or notice premarket approval premarket notifica premarket notification procedures procedures in Subpart protein reagents reagents are devices reclassification request requirement for premarket safety and effectiveness Sept serological serological reagents serum sponsor statement submitted surgical test sys tigational tion procedures tissue trols tube urine user facility vice
Populāri fragmenti
561. lappuse - That all charges for storage, cartage and labor on goods which are refused admission or delivery shall be paid by the owner or consignee, and in default of such payment shall constitute a...
15. lappuse - The failure of the label to extend over the area of the container or package available for such extension, so as to provide sufficient label space for the prominent placing of such word, statement, or information; (4) Insufficiency of label space for the prominent placing of such word, statement, or information, resulting from 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; (5) Insufficiency of label...
21. lappuse - Act (1) small open containers of fresh fruits and fresh vegetables and (2) food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such food is not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, or repacking establishment.
98. lappuse - An identifying lot or control number from which it is possible to determine the complete manufacturing history of the package of the drug...
546. 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.
60. lappuse - ... permit any authorized FDA employee at all reasonable times to have access to, and to copy and verify, the records contained in this file.
549. lappuse - Administration designated in the notice and shall be private and confined to questions of fact. The parties notified may present evidence, either oral or written, in person or by attorney, to show cause why the matter should not be referred for prosecution as a violation of the Federal Caustic Poison Act.
52. lappuse - ... similar device marketed by the manufacturer or importer would be likely to cause or contribute to a death or serious injury if the malfunction were to recur; (2) shall define the term "serious injury...
94. lappuse - label" means a display of written, printed, or graphic matter upon the immediate container of any substance; and a requirement made by or under authority of this Act that any word, statement, or other information appear on the label shall not be considered to be complied with unless such word, statement, or other information also appears...
83. lappuse - Except as provided in subsection (b), no State or political subdivision of a State may establish or continue in effect...