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Pubmed for Handhelds
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Journal Abstract Search
257 related items for PubMed ID: 10122957
1. The FDA moves to implement the Safe Medical Devices Act. Tamborlane T. Healthspan; 1992 Nov; 9(10):7-10. PubMed ID: 10122957 [No Abstract] [Full Text] [Related]
3. The Safe Medical Devices Act. Williams MA. South Hosp; 1992 Nov; 58(2):16-7. PubMed ID: 10118188 [Abstract] [Full Text] [Related]
4. AHA comments to FDA on Safe Devices Act. DePorter J. Mater Manag Health Care; 1992 Apr; 1(2):18-21. PubMed ID: 10125489 [No 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 16; 58(156):43442-51. PubMed ID: 10127886 [Abstract] [Full Text] [Related]
12. Update on the Safe Medical Devices Act of 1990: current hospital requirements and recommended actions 1996. Berek B. Healthc Facil Manag Ser; 1996 Jul 16; ():1-18. PubMed ID: 10159144 [Abstract] [Full Text] [Related]
14. Medical device reports raise and red flag. Miles F, Miles JF. Provider; 1997 Jan 16; 23(1):53, 55-6. PubMed ID: 10166155 [No Abstract] [Full Text] [Related]
15. AHA objects to key parts of device regulations. DePorter J. Health Facil Manage; 1992 Apr 16; 5(4):38, 40, 42 passim. PubMed ID: 10116728 [Abstract] [Full Text] [Related]
16. Developing a comprehensive program to implement the Safe Medical Devices Act. Reissland G. QRC Advis; 1995 Sep 16; 11(11):1-5. PubMed ID: 10144951 [No Abstract] [Full Text] [Related]
17. 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 01; 58(168):46514-23. PubMed ID: 10128335 [Abstract] [Full Text] [Related]
18. 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]
19. New medical devices reporting requirements. Carley MM. Contemp Longterm Care; 1991 Dec 26; 14(12):66, 68. PubMed ID: 10117951 [No Abstract] [Full Text] [Related]