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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 10110321)

  • 21. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration; correction--FDA. Tentative final rule; correction.
    Fed Regist; 1992 Feb; 57(37):6486-7. PubMed ID: 10117356
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Medical device incident investigation.
    Baretich MF
    Biomed Sci Instrum; 2007; 43():302-5. PubMed ID: 17487098
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hospitals wary of interpretation of medical device reporting law.
    Burke M
    Hospitals; 1991 Oct; 65(20):40, 42. PubMed ID: 1916713
    [No Abstract]   [Full Text] [Related]  

  • 24. The Feds do it again. The EMS community grows wary--and weary--of FDA intervention.
    Nordberg M
    Emerg Med Serv; 1995 Mar; 24(3):40-52. PubMed ID: 10140757
    [No Abstract]   [Full Text] [Related]  

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

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

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

  • 28. Medical device surveillance world-wide.
    Badea C; Kolitsi Z; Pallikarakis N; Papapanagiotou A
    Stud Health Technol Inform; 1996; 28():157-74. PubMed ID: 10184634
    [No Abstract]   [Full Text] [Related]  

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

  • 30. 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; 61(71):16043-5. PubMed ID: 10157704
    [No Abstract]   [Full Text] [Related]  

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

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

  • 33. Sharps containers classified as medical devices.
    Healthc Hazard Mater Manage; 1993 Mar; 6(6):9-10. PubMed ID: 10124549
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. What you should know about device recalls.
    OR Manager; 2002 Apr; 18(4):21. PubMed ID: 11962164
    [No Abstract]   [Full Text] [Related]  

  • 36. US Congress considers new tracking system for medical devices after excessive recalls.
    Epstein K
    BMJ; 2012 Apr; 344():e2915. PubMed ID: 22529316
    [No Abstract]   [Full Text] [Related]  

  • 37. Hospital expands tracking system to comply with law.
    Gooch DA
    OR Manager; 1994 Apr; 10(4):16-7. PubMed ID: 10133245
    [No Abstract]   [Full Text] [Related]  

  • 38. Device tracking: what's covered? How'll it work?
    Muehlbauer EJ
    Health Facil Manage; 1992 Oct; 5(10):40, 42-3. PubMed ID: 10121451
    [No Abstract]   [Full Text] [Related]  

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

  • 40. Should hospitals report to the FDA?
    McNaughton DJ
    Healthc Comput Commun; 1987 Oct; 4(10):29. PubMed ID: 10288562
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.