210 related articles for article (PubMed ID: 10117356)
1. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration; correction--FDA. Tentative final rule; correction.
Fed Regist; 1992 Feb; 57(37):6486-7. PubMed ID: 10117356
[TBL] [Abstract][Full Text] [Related]
2. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration--FDA. Tentative final rule.
Fed Regist; 1991 Nov; 56(228):60024-39. PubMed ID: 10115705
[TBL] [Abstract][Full Text] [Related]
3. Medical devices; medical device distributor reporting--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
Fed Regist; 1993 Sep; 58(168):46514-23. PubMed ID: 10128335
[TBL] [Abstract][Full Text] [Related]
4. Medical devices; medical device distributor reporting; opportunity for comments--FDA. Final rule; opportunity for comments.
Fed Regist; 1993 Sep; 58(168):46514. PubMed ID: 10128334
[TBL] [Abstract][Full Text] [Related]
5. 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; 58(156):43442-51. PubMed ID: 10127886
[TBL] [Abstract][Full Text] [Related]
6. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
Fed Regist; 1998 May; 63(91):26069-77. PubMed ID: 10179334
[TBL] [Abstract][Full Text] [Related]
7. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Jan; 65(17):4112-21. PubMed ID: 11010653
[TBL] [Abstract][Full Text] [Related]
8. Medical devices; device tracking--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
Fed Regist; 1992 May; 57(104):22966-70. PubMed ID: 10171013
[TBL] [Abstract][Full Text] [Related]
9. Medical devices: reports of corrections and removals; delay of effective data--FDA. Direct final rule; delay of effective date.
Fed Regist; 1998 Nov; 63(222):63983. PubMed ID: 10339047
[TBL] [Abstract][Full Text] [Related]
10. Medical devices; reports of corrections and removals; companion to direct final rule--FDA. Proposed rule.
Fed Regist; 1998 Aug; 63(152):42300-4. PubMed ID: 10181727
[TBL] [Abstract][Full Text] [Related]
11. Facilities strive to comply with new Act. The long-term effects of the Safe Medical Devices Act are still unknown.
Schuster DK; Butler KH
Health Prog; 1993 May; 74(4):53-7. PubMed ID: 10125364
[TBL] [Abstract][Full Text] [Related]
12. Medical devices; medical device user facility and manufacturer reporting, certification and registration; Office of Management and Budget approval; extension of effective date--FDA. Final rule; notification of approval of information collection requirements.
Fed Regist; 1996 Apr; 61(71):16043-5. PubMed ID: 10157704
[No Abstract] [Full Text] [Related]
13. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
Alder HC
Hosp Technol Ser; 1993 Oct; 12(11):1-27. PubMed ID: 10129209
[TBL] [Abstract][Full Text] [Related]
14. Medical device reporting for user facilities.
Radiol Manage; 1992; 14(4):65-70. PubMed ID: 10123092
[TBL] [Abstract][Full Text] [Related]
15. Medical devices; reports of corrections and removals--FDA. Direct final rule.
Fed Regist; 1998 Aug; 63(152):42229-33. PubMed ID: 10181725
[TBL] [Abstract][Full Text] [Related]
16. Medical devices; establishment registration and device listing for manufacturers and distributors of devices; correction--FDA. Direct final rule; correction.
Fed Regist; 1998 Nov; 63(228):65554-5. PubMed ID: 10338874
[TBL] [Abstract][Full Text] [Related]
17. AHA objects to key parts of device regulations.
DePorter J
Health Facil Manage; 1992 Apr; 5(4):38, 40, 42 passim. PubMed ID: 10116728
[TBL] [Abstract][Full Text] [Related]
18. Postmarket surveillance. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Jun; 67(109):38878-92. PubMed ID: 12053947
[TBL] [Abstract][Full Text] [Related]
19. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Direct final rule; withdrawal.
Fed Regist; 1998 Aug; 63(154):42699. PubMed ID: 10182563
[TBL] [Abstract][Full Text] [Related]
20. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting--FDA. Direct final rule; withdrawal.
Fed Regist; 1998 Aug; 63(166):45716-7. PubMed ID: 10182694
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
