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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

148 related items for PubMed ID: 470665

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. FDA's developing standards policy.
    Link DM.
    Med Instrum; 1979; 13(4):196-7. PubMed ID: 470656
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
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  • 4. FDA's focus on consensus standards: the vision, the heartbreak, the hope.
    Altman MR, Marlowe DE.
    Stand News; 1999 May; 27(5):24-5. PubMed ID: 10558422
    [No Abstract] [Full Text] [Related]

  • 5. FDA's medical device standards policy.
    Stimson RA.
    J Parenter Sci Technol; 1981 May; 35(2):60-2. PubMed ID: 7229834
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
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  • 7. [Standards used in the regulation of medical device in USA].
    Hu W, Gu H.
    Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2007 Nov; 21(11):1263-7. PubMed ID: 18069490
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
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  • 9. Using the FDA's Device Experience Network.
    Collins JL.
    Oncol Nurs Forum; 1992 Apr; 19(3):524. PubMed ID: 1594477
    [No Abstract] [Full Text] [Related]

  • 10.
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  • 11. FDA's Quality System Inspection Technique in Ireland.
    Higgins S.
    Med Device Technol; 2001 Apr; 12(1):40-1. PubMed ID: 11317865
    [No Abstract] [Full Text] [Related]

  • 12. Medical devices; procedures for premarket notification, premarket approval, classification, performance standards establishment, banning devices, and availability of regulatory hearings--FDA. Final rule.
    Fed Regist; 1992 Dec 10; 57(238):58400-6. PubMed ID: 10123143
    [Abstract] [Full Text] [Related]

  • 13. The Safe Medical Devices Act of 1990--FDA. Notice.
    Fed Regist; 1991 Apr 05; 56(66):14111-3. PubMed ID: 10111151
    [Abstract] [Full Text] [Related]

  • 14. FDA's performance standard for electrode lead wires and patient cables. Second phase is now being implemented.
    Health Devices; 2000 Apr 05; 29(4):140-1. PubMed ID: 11002440
    [No Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. ECRI to clinical engineering departments: "heads up! ... FDA's potential regulation of servicers, remarketers, and refurbishers could affect you".
    Health Devices; 1998 Aug 10; 27(8):276. PubMed ID: 9743899
    [No Abstract] [Full Text] [Related]

  • 17. The FDA's final regulations: IRBs and medical devices.
    Holder AR.
    IRB; 1980 Aug 10; 2(6):1-4. PubMed ID: 11661803
    [No Abstract] [Full Text] [Related]

  • 18. 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 24; 65(15):3584-5. PubMed ID: 11010654
    [Abstract] [Full Text] [Related]

  • 19. FDA's proposed regulatory approach to regulation of hematopoietic stem/progenitor cell products.
    Harvath L.
    Cytotherapy; 1999 Jan 24; 1(4):358-9. PubMed ID: 20440912
    [No Abstract] [Full Text] [Related]

  • 20. Upon closer inspection. As the U.S. imports more drugs and devices, the FDA's overseas initiatives aim to head off trouble at the source.
    Rhea S.
    Mod Healthc; 2009 Mar 30; 39(13):28-30. PubMed ID: 19405431
    [No Abstract] [Full Text] [Related]

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