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4. Neurosurgical devices and drugs: The Medical Device Amendments of 1976. Burton CV Neurosurgery; 1978; 2(1):74-5. PubMed ID: 683484 [No Abstract] [Full Text] [Related]
5. Standards for medical devices. Wickstrom J South Med J; 1976 Sep; 69(9):1247. PubMed ID: 968554 [No Abstract] [Full Text] [Related]
6. 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]
7. Health device legislation: an overview of the law and its impact on respiratory care. Bancroft ML; Steen JA Respir Care; 1978 Dec; 23(12):1179-84. PubMed ID: 10315033 [TBL] [Abstract][Full Text] [Related]
8. Who will regulate devices? Nurses and hospitals. Lewis HL Mod Hosp; 1973 Nov; 121(5):74-6. PubMed ID: 4786790 [No Abstract] [Full Text] [Related]
9. Equipment standards: history, litigation, and advice. Hedley-Whyte J; Milamed DR Ann Surg; 1999 Jul; 230(1):120-7. PubMed ID: 10400045 [TBL] [Abstract][Full Text] [Related]
10. Amendment of various device regulations to reflect current American Society for Testing and Material citations. Food and Drug Administration, HHS. Direct final rule. Fed Regist; 2000 Jan; 65(15):3584-5. PubMed ID: 11010654 [TBL] [Abstract][Full Text] [Related]
11. Medical device legislation. Miller MJ Hospitals; 1973 Jun; 47(11):81-8. PubMed ID: 4706560 [No Abstract] [Full Text] [Related]
12. Fighting trafficking of falsified and substandard medicinal products in Russia. Fayzrakhmanov NF Int J Risk Saf Med; 2015; 27 Suppl 1():S37-40. PubMed ID: 26639702 [TBL] [Abstract][Full Text] [Related]
13. A nobleness of purpose. The 1980 AANS presidential address. Stern WE J Neurosurg; 1980 Aug; 53(2):137-43. PubMed ID: 7431053 [TBL] [Abstract][Full Text] [Related]
15. Classification of medical devices and priorities in standards-setting in the United States. Laufman H Med Instrum; 1977; 11(3):180-2. PubMed ID: 875768 [No Abstract] [Full Text] [Related]
16. The "déjà vu effect:" evaluation of United States medical device legislation, regulation, and the Food and Drug Administration's contentious 510(k) program. Bauman J Food Drug Law J; 2012; 67(3):337-61, i. PubMed ID: 24624654 [TBL] [Abstract][Full Text] [Related]
17. U.S. Food and Drug Administration and regulation of medical devices in radiology. Pritchard WF; Carey RF Radiology; 1997 Oct; 205(1):27-36. PubMed ID: 9314955 [TBL] [Abstract][Full Text] [Related]
18. Medical Device Amendments of 1976. Greenberg RB Am J Hosp Pharm; 1976 Dec; 33(12):1308-11. PubMed ID: 998650 [TBL] [Abstract][Full Text] [Related]
19. Medical devices; exemption from premarket notification requirements; class I devices; technical amendment. Final rule; technical amendment. Food and Drug Administration. HHS Fed Regist; 2001 Jul; 66(143):38786-819. PubMed ID: 11725800 [TBL] [Abstract][Full Text] [Related]
20. The Ear, Nose, and Throat Devices Classification Panel of the Food And Drug Administration. Naunton RF; Sauberman HR Otolaryngol Head Neck Surg (1979); 1979; 87(1):27-31. PubMed ID: 503469 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]