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PUBMED FOR HANDHELDS

Journal Abstract Search


153 related items for PubMed ID: 9743899

  • 1. ECRI to clinical engineering departments: "heads up! ... FDA's potential regulation of servicers, remarketers, and refurbishers could affect you".
    Health Devices; 1998 Aug; 27(8):276. PubMed ID: 9743899
    [No Abstract] [Full Text] [Related]

  • 2. Secondhand woes. FDA rethinking the rules on refurbished devices. What could that mean for you?
    Gwynne P.
    Health Facil Manage; 1998 Nov; 11(11):46, 48, 50-2. PubMed ID: 10345426
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  • 7. Using the FDA's Device Experience Network.
    Collins JL.
    Oncol Nurs Forum; 1992 Apr; 19(3):524. PubMed ID: 1594477
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  • 8. FDA's developing standards policy.
    Link DM.
    Med Instrum; 1979 Apr; 13(4):196-7. PubMed ID: 470656
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  • 10. Voluntary consensus standards and the FDA's regulatory program.
    Gardner S.
    Med Instrum; 1979 Apr; 13(4):239-42. PubMed ID: 470665
    [No Abstract] [Full Text] [Related]

  • 11. Delegations of authority and organization; Center for Devices and Radiological Health--FDA. Final rule.
    Fed Regist; 1991 Oct 10; 56(197):51169-70. PubMed ID: 10115059
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  • 12. Medical devices; refurbishers, rebuilders, reconditioners, servicers, and "as is" remarketers of medical devices; review and revision of compliance policy guides and regulatory requirements; request for comments and information--FDA. Advance notice of proposed rulemaking.
    Fed Regist; 1997 Dec 23; 62(246):67011-3. PubMed ID: 10179309
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  • 15. Medical devices; reconditioners, rebuilders of medical devices; revocation of compliance policy guide; request for comments--FDA. Notice.
    Fed Regist; 1998 Dec 04; 63(233):67076-8. PubMed ID: 10338883
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  • 17. Is FDA's medical device evaluation process overly complaisant to industry?
    Margolis RE.
    Healthspan; 1992 Dec 04; 9(7):19-20. PubMed ID: 10121440
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  • 18. Proposed FDA "unsafe" lead wire ban could affect many medical devices.
    Hosp Technol Ser; 1995 Jul 04; 14(7):12-4. PubMed ID: 10144657
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  • 19. Medical devices; medical device reporting. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2005 Feb 28; 70(38):9516-28. PubMed ID: 15736310
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