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. |
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1.–5. rezultāts no 46.
4. lappuse
... Importation of electronic products ....... 505 1010 Performance standards for electronic products : general ...... 509 1020 Performance standards for ionizing radiation emit- ting products ...... 514 1030 Performance standards for ...
... Importation of electronic products ....... 505 1010 Performance standards for electronic products : general ...... 509 1020 Performance standards for ionizing radiation emit- ting products ...... 514 1030 Performance standards for ...
26. lappuse
... importer for resale . Such importer may have the tests required by paragraph ( d ) of this section conducted in the country of origin but must make the results thereof available , upon request , to the Food and Drug Administration , as ...
... importer for resale . Such importer may have the tests required by paragraph ( d ) of this section conducted in the country of origin but must make the results thereof available , upon request , to the Food and Drug Administration , as ...
56. lappuse
... importer to report to FDA whenever the manufacturer or importer receives or other- wise becomes aware of information that rea- sonably suggests that one of its marketed devices ( 1 ) may have caused or contributed to a death or serious ...
... importer to report to FDA whenever the manufacturer or importer receives or other- wise becomes aware of information that rea- sonably suggests that one of its marketed devices ( 1 ) may have caused or contributed to a death or serious ...
57. lappuse
... importer shall sub- mit to FDA a report containing the informa- tion listed in paragraph ( c ) of this section whenever the manufacturer or importer : ( 1 ) Receives or otherwise becomes aware of oral or written information that ...
... importer shall sub- mit to FDA a report containing the informa- tion listed in paragraph ( c ) of this section whenever the manufacturer or importer : ( 1 ) Receives or otherwise becomes aware of oral or written information that ...
58. lappuse
... importer , including ( i ) whether any deaths or serious injuries have occurred and ( ii ) the number of persons who died or were seriously injured . ( If the re- port is required under paragraph ( a ) ( 2 ) ( 1 ) of this section , the ...
... importer , including ( i ) whether any deaths or serious injuries have occurred and ( ii ) the number of persons who died or were seriously injured . ( If the re- port is required under paragraph ( a ) ( 2 ) ( 1 ) of this section , the ...
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Bieži izmantoti vārdi un frāzes
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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...