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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

354 related items for PubMed ID: 10171013

  • 1. Medical devices; device tracking--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
    Fed Regist; 1992 May 29; 57(104):22966-70. PubMed ID: 10171013
    [Abstract] [Full Text] [Related]

  • 2. Medical devices; device tracking--FDA. Final rule; suspension of effective date; notification of status under the Safe Medical Devices Act; technical amendments.
    Fed Regist; 1993 Aug 16; 58(156):43442-51. PubMed ID: 10127886
    [Abstract] [Full Text] [Related]

  • 3. Medical devices; medical device distributor reporting--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
    Fed Regist; 1993 Sep 01; 58(168):46514-23. PubMed ID: 10128335
    [Abstract] [Full Text] [Related]

  • 4. Medical devices; illustrative and designated lists for device tracking--FDA. Final rule and request for comments.
    Fed Regist; 1993 Aug 16; 58(156):43451-5. PubMed ID: 10171508
    [Abstract] [Full Text] [Related]

  • 5. Medical devices; medical device distributor reporting; opportunity for comments--FDA. Final rule; opportunity for comments.
    Fed Regist; 1993 Sep 01; 58(168):46514. PubMed ID: 10128334
    [Abstract] [Full Text] [Related]

  • 6. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration--FDA. Tentative final rule.
    Fed Regist; 1991 Nov 26; 56(228):60024-39. PubMed ID: 10115705
    [Abstract] [Full Text] [Related]

  • 7. Medical devices; reports of corrections and removals--FDA. Final rule.
    Fed Regist; 1997 May 19; 62(96):27183. PubMed ID: 10167533
    [Abstract] [Full Text] [Related]

  • 8. Medical devices; device tracking; new orders to manufacturers--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10638-40. PubMed ID: 10177504
    [Abstract] [Full Text] [Related]

  • 9. Medical devices; reports of corrections and removals; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Aug 07; 63(152):42300-4. PubMed ID: 10181727
    [Abstract] [Full Text] [Related]

  • 10. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
    Alder HC.
    Hosp Technol Ser; 1993 Oct 07; 12(11):1-27. PubMed ID: 10129209
    [Abstract] [Full Text] [Related]

  • 11. Medical devices; reports of corrections and removals--FDA. Direct final rule.
    Fed Regist; 1998 Aug 07; 63(152):42229-33. PubMed ID: 10181725
    [Abstract] [Full Text] [Related]

  • 12. Medical devices; establishment registration and device listing for manufacturers and distributors of devices; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Sep 29; 63(188):51874-5. PubMed ID: 10185813
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Medical devices: reports of corrections and removals; delay of effective data--FDA. Direct final rule; delay of effective date.
    Fed Regist; 1998 Nov 18; 63(222):63983. PubMed ID: 10339047
    [Abstract] [Full Text] [Related]

  • 15. Medical devices; exemption from premarket notification and reserved devices; class I. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan 14; 65(10):2296-323. PubMed ID: 11010655
    [Abstract] [Full Text] [Related]

  • 16. FDA modernization act of 1997: guidance on medical device tracking; availability--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10640-1. PubMed ID: 10177505
    [Abstract] [Full Text] [Related]

  • 17. Medical devices; humanitarian use of devices; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr 17; 63(74):19196-200. PubMed ID: 10178431
    [Abstract] [Full Text] [Related]

  • 18. Medical devices; establishment registration and device listing for manufacturers and distributors of devices--FDA. Direct final rule.
    Fed Regist; 1998 Sep 29; 63(188):51825-7. PubMed ID: 10185812
    [Abstract] [Full Text] [Related]

  • 19. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20558-61. PubMed ID: 10179320
    [Abstract] [Full Text] [Related]

  • 20. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
    Fed Regist; 1998 May 12; 63(91):26069-77. PubMed ID: 10179334
    [Abstract] [Full Text] [Related]

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