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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
187 related items for PubMed ID: 10155771
1. New FDA reporting rule means new concerns. Healthc Hazard Mater Manage; 1996 Mar; 9(6):1-4. PubMed ID: 10155771 [No Abstract] [Full Text] [Related]
2. 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. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration; correction--FDA. Tentative final rule; correction. Fed Regist; 1992 Feb 25; 57(37):6486-7. PubMed ID: 10117356 [Abstract] [Full Text] [Related]
5. Medical device reporting for user facilities. Radiol Manage; 1992 Feb 25; 14(4):65-70. PubMed ID: 10123092 [Abstract] [Full Text] [Related]
6. Medical devices act means more paperwork. Patterson P. OR Manager; 1991 Mar 25; 7(3):18-9. PubMed ID: 10109904 [No Abstract] [Full Text] [Related]
7. 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 25; 74(4):53-7. PubMed ID: 10125364 [Abstract] [Full Text] [Related]
8. AHA objects to key parts of device regulations. DePorter J. Health Facil Manage; 1992 Apr 25; 5(4):38, 40, 42 passim. PubMed ID: 10116728 [Abstract] [Full Text] [Related]
9. 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]
10. FDA issues new rule on medical device reporting. OR Manager; 1996 Feb 26; 12(2):1, 7-8. PubMed ID: 10154766 [No Abstract] [Full Text] [Related]
11. 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]
12. AHA comments to FDA on Safe Devices Act. DePorter J. Mater Manag Health Care; 1992 Apr 26; 1(2):18-21. PubMed ID: 10125489 [No Abstract] [Full Text] [Related]
13. Medical device reports raise and red flag. Miles F, Miles JF. Provider; 1997 Jan 26; 23(1):53, 55-6. PubMed ID: 10166155 [No Abstract] [Full Text] [Related]
14. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting. Food and Drug Administration, HHS. Final rule. Fed Regist; 2000 Jan 26; 65(17):4112-21. PubMed ID: 11010653 [Abstract] [Full Text] [Related]
15. 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]
16. Questions and answers about tracking program. OR Manager; 1994 Apr 12; 10(4):13-4. PubMed ID: 10133243 [No Abstract] [Full Text] [Related]
17. Facilities' responsibilities after notification of a medical device hazard or recall. Health Devices; 2004 Sep 12; 33(9):339. PubMed ID: 15532863 [No Abstract] [Full Text] [Related]
18. Safe Medical Devices Act of 1990: current hospital requirements and recommended actions. Alder H. Healthc Facil Manag Ser; 1993 Sep 12; ():1-34. PubMed ID: 10132639 [Abstract] [Full Text] [Related]
19. The safe Medical Devices Act of 1990--a look at the implications. Interview by Larry Tanner. Reynolds C, Allen E, Lipschultz A, Pilot L, Solomon R. Biomed Instrum Technol; 1991 Sep 12; 25(5):347-50, 352-60. PubMed ID: 1933085 [No Abstract] [Full Text] [Related]
20. Impact of the Safe Medical Devices Act on healthcare facilities. Lekhy C. J Healthc Qual; 1993 Sep 12; 15(1):36-8. PubMed ID: 10123341 [Abstract] [Full Text] [Related] Page: [Next] [New Search]