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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

253 related items for PubMed ID: 10116728

  • 1. AHA objects to key parts of device regulations.
    DePorter J.
    Health Facil Manage; 1992 Apr; 5(4):38, 40, 42 passim. PubMed ID: 10116728
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 5. 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]

  • 6. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
    Alder HC.
    Hosp Technol Ser; 1993 Oct 16; 12(11):1-27. PubMed ID: 10129209
    [Abstract] [Full Text] [Related]

  • 7. Medical device reporting for user facilities.
    Radiol Manage; 1992 Oct 16; 14(4):65-70. PubMed ID: 10123092
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  • 8. 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]

  • 9. 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]

  • 10. 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]

  • 11. The Safe Medical Devices Act.
    Williams MA.
    South Hosp; 1992 Feb 25; 58(2):16-7. PubMed ID: 10118188
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Facilities strive to comply with new Act. The long-term effects of the Safe Medical Devices Act are still unknown.
    Schuster DK, Butler KH.
    Health Prog; 1993 May 16; 74(4):53-7. PubMed ID: 10125364
    [Abstract] [Full Text] [Related]

  • 14. Medical device reporting: the US final rule.
    Donawa ME.
    Med Device Technol; 1996 Mar 16; 7(2):14-6, 18, 20-1. PubMed ID: 10159867
    [Abstract] [Full Text] [Related]

  • 15. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan 26; 65(17):4112-21. PubMed ID: 11010653
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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]

  • 18. 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]

  • 19. Medical device recall authority--FDA. Final rule.
    Fed Regist; 1996 Nov 20; 61(225):59004-22. PubMed ID: 10163116
    [Abstract] [Full Text] [Related]

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