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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

345 related items for PubMed ID: 10160028

  • 1. Are you ready? FDA final rules on devices are on the way.
    Berek B.
    Health Facil Manage; 1996 Sep; 9(9):56, 58, 60 passim. PubMed ID: 10160028
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. Recent legal developments affecting medical device manufacturers.
    Lough MH.
    Healthspan; 1993 Sep 16; 10(8):21-3. PubMed ID: 10129148
    [No Abstract] [Full Text] [Related]

  • 6. Medical devices; medical device user facility and manufacturer reporting, certification and registration; Office of Management and Budget approval; extension of effective date--FDA. Final rule; notification of approval of information collection requirements.
    Fed Regist; 1996 Apr 11; 61(71):16043-5. PubMed ID: 10157704
    [No Abstract] [Full Text] [Related]

  • 7. Safe Devices II: meeting the Act's tracking portion.
    Alder HC.
    Mater Manag Health Care; 1993 Dec 11; 2(12):34, 36, 38. PubMed ID: 10130500
    [No Abstract] [Full Text] [Related]

  • 8. Ensuring safe and effective medical devices.
    Feigal DW, Gardner SN, McClellan M.
    N Engl J Med; 2003 Jan 16; 348(3):191-2. PubMed ID: 12529457
    [No Abstract] [Full Text] [Related]

  • 9. Postmarketing surveillance of medical devices using Medicare claims.
    Malenka DJ, Kaplan AV, Sharp SM, Wennberg JE.
    Health Aff (Millwood); 2005 Jan 16; 24(4):928-37. PubMed ID: 16012135
    [Abstract] [Full Text] [Related]

  • 10. Medical device reporting for user facilities.
    Radiol Manage; 1992 Jan 16; 14(4):65-70. PubMed ID: 10123092
    [Abstract] [Full Text] [Related]

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

  • 12. FDA works to reduce preventable medical device injuries.
    Rados C.
    FDA Consum; 2003 Jan 16; 37(4):29-33. PubMed ID: 12971346
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Medical device vigilance at FDA.
    Gross TP, Kessler LG.
    Stud Health Technol Inform; 1996 Aug 16; 28():17-24. PubMed ID: 10164091
    [Abstract] [Full Text] [Related]

  • 15. Postmarket surveillance. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Jun 06; 67(109):38878-92. PubMed ID: 12053947
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. FDA issues new rule on medical device reporting.
    OR Manager; 1996 Feb 06; 12(2):1, 7-8. PubMed ID: 10154766
    [No Abstract] [Full Text] [Related]

  • 18. Medical device epidemiology and surveillance: patient safety is the bottom line.
    Brown SL, Bright RA, Tavris DR.
    Expert Rev Med Devices; 2004 Sep 06; 1(1):1-2. PubMed ID: 16293003
    [No Abstract] [Full Text] [Related]

  • 19. Form for reporting serious adverse events and product problems with human drug and biological products and devices; availability--FDA. Notice.
    Fed Regist; 1993 Jun 03; 58(105):31596-614. PubMed ID: 10171452
    [Abstract] [Full Text] [Related]

  • 20. 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]

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