These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

149 related items for PubMed ID: 470656

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

  • 2. Voluntary consensus standards and the FDA's regulatory program.
    Gardner S.
    Med Instrum; 1979; 13(4):239-42. PubMed ID: 470665
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Voluntary standards: development and use.
    Miller MJ.
    Med Instrum; 1979; 13(4):203-6. PubMed ID: 470660
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Is FDA's medical device evaluation process overly complaisant to industry?
    Margolis RE.
    Healthspan; 1992; 9(7):19-20. PubMed ID: 10121440
    [No Abstract] [Full Text] [Related]

  • 8. 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]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. The FDA's policy on the regulation of computerized medical devices.
    Furfine CS.
    MD Comput; 1992 Apr; 9(2):97-100. PubMed ID: 1573995
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 17. 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]

  • 18. Implications of the 1976 medical devices legislation.
    Banta D, Brown S, Behney C.
    Man Med; 1978 Jan 24; 3(2):131-43. PubMed ID: 10316645
    [No Abstract] [Full Text] [Related]

  • 19. FDA's standards policy for medical devices.
    Stimson RA.
    AORN J; 1980 Aug 24; 32(2):214-8. PubMed ID: 6904175
    [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]

    Page: [Next] [New Search]
    of 8.