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4. Medical devices; illustrative and designated lists for device tracking--FDA. Final rule and request for comments. Fed Regist; 1993 Aug 16; 58(156):43451-5. PubMed ID: 10171508 [Abstract] [Full Text] [Related]
7. Medical devices; device tracking--FDA. Final rule; suspension of effective date; notification of status under the Safe Medical Devices Act; technical amendments. Fed Regist; 1993 Aug 16; 58(156):43442-51. PubMed ID: 10127886 [Abstract] [Full Text] [Related]
9. Medical devices; implementation of third party review under the Food and Drug Administration Modernization Act of 1997; emergency processing request under OMB review--FDA. Notice. Fed Regist; 1998 May 22; 63(99):28388-91. PubMed ID: 10179874 [Abstract] [Full Text] [Related]
11. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule. Fed Regist; 1998 May 12; 63(91):26069-77. PubMed ID: 10179334 [Abstract] [Full Text] [Related]
12. Medical devices; medical device distributor reporting; opportunity for comments--FDA. Final rule; opportunity for comments. Fed Regist; 1993 Sep 01; 58(168):46514. PubMed ID: 10128334 [Abstract] [Full Text] [Related]
14. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration--FDA. Tentative final rule. Fed Regist; 1991 Nov 26; 56(228):60024-39. PubMed ID: 10115705 [Abstract] [Full Text] [Related]
16. Medical devices; exemptions from premarket notification; class II devices--FDA, Final rule. Fed Regist; 1998 Nov 03; 63(212):59222-31. PubMed ID: 10187384 [Abstract] [Full Text] [Related]
18. Medical devices; reports of corrections and removals; companion to direct final rule--FDA. Proposed rule. Fed Regist; 1998 Aug 07; 63(152):42300-4. PubMed ID: 10181727 [Abstract] [Full Text] [Related]