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3. The Safe Medical Devices Act. Williams MA. South Hosp; 1992; 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]
18. Safe Medical Devices Act of 1990: current hospital requirements and recommended actions. Alder H. Healthc Facil Manag Ser; 1993 Sep 25; ():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 25; 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 25; 15(1):36-8. PubMed ID: 10123341 [Abstract] [Full Text] [Related] Page: [Next] [New Search]