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 *

133 related articles for article (PubMed ID: 7288982)

  • 1. FDA approves more medical devices.
    JAMA; 1981 Nov; 246(18):2014. PubMed ID: 7288982
    [No Abstract]   [Full Text] [Related]  

  • 2. Characteristics of Clinical Studies Conducted Over the Total Product Life Cycle of High-Risk Therapeutic Medical Devices Receiving FDA Premarket Approval in 2010 and 2011.
    Rathi VK; Krumholz HM; Masoudi FA; Ross JS
    JAMA; 2015 Aug; 314(6):604-12. PubMed ID: 26262798
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Safety standards. The FDA withdraws its notices of intent to mandate safety standards for electromedical devices.
    Schwartz AP
    Med Electron; 1989 Feb; 20(1):120-1. PubMed ID: 10292029
    [No Abstract]   [Full Text] [Related]  

  • 4. FDA approval and surveillance of medical devices.
    Graham AA
    AANA J; 1987 Feb; 55(1):59-64. PubMed ID: 3645951
    [No Abstract]   [Full Text] [Related]  

  • 5. Radiology devices; general provisions and classifications of 59 devices--FDA. Final rule.
    Fed Regist; 1988 Jan; 53(12):1554-71. PubMed ID: 10285636
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Order for transitional class III devices; submission of safety and effectiveness information under section 520(1)(5)(A) of the Federal Food, Drug, and Cosmetic Act--FDA. Notice.
    Fed Regist; 1991 Nov; 56(220):57960-3. PubMed ID: 10115560
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Policy statement; class II medical devices--FDA. Notice.
    Fed Regist; 1985 Oct; 50(205):43060-81. PubMed ID: 10274028
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Medical devices; various proposed rules for device classification; withdrawal of proposed rules. Food and Drug Administration. Withdrawal of proposed rules.
    Fed Regist; 1982 Mar; 47(54):11880-2. PubMed ID: 10254383
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Medical devices, the FDA, and the home healthcare clinician.
    Simone LK; Brumbaugh J; Ricketts C
    Home Healthc Nurse; 2014; 32(7):402-8. PubMed ID: 24978574
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FDA "approval" of medical devices.
    Health Devices; 1999; 28(5-6):235. PubMed ID: 10412079
    [No Abstract]   [Full Text] [Related]  

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

  • 12. Delegations of authority and organization; Center for Devices and Radiological Health--FDA. Final rule.
    Fed Regist; 1991 Oct; 56(197):51169-70. PubMed ID: 10115059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FDA issues final guidance on requirements governing single-use medical devices.
    Rep Med Guidel Outcomes Res; 2000 Sep; 11(19):5-6. PubMed ID: 11865892
    [No Abstract]   [Full Text] [Related]  

  • 14. Medical devices; medical device reporting; baseline reports; stay of effective date--FDA. Final rule.
    Fed Regist; 1996 Jul; 61(148):39868-9. PubMed ID: 10159600
    [No Abstract]   [Full Text] [Related]  

  • 15. FDA working to ensure the safety of medical devices used in the pediatric population.
    Flack MN; Gross TP; Reid JS; Mills TT; Francis J
    Pediatr Clin North Am; 2012 Dec; 59(6):1355-66. PubMed ID: 23116531
    [TBL] [Abstract][Full Text] [Related]  

  • 16. FDA marketing claims, and the practitioner.
    Runner S
    J Evid Based Dent Pract; 2006 Mar; 6(1):19-23. PubMed ID: 17138391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Medical devices; exemptions from premarket notification and reserved devices; class I--FDA. Notice.
    Fed Regist; 1998 Feb; 63(21):5387-93. PubMed ID: 10177333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The financing and regulation of medical devices in the United States.
    Sisk JE
    Med Prog Technol; 1982; 9(2-3):181-6. PubMed ID: 7162490
    [TBL] [Abstract][Full Text] [Related]  

  • 19. FDA announces final rule establishing UDI system for medical devices.
    Health Devices; 2013 Nov; 42(11):383. PubMed ID: 24358514
    [No Abstract]   [Full Text] [Related]  

  • 20. Medical devices; humanitarian use of devices--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Jul; 63(147):40825. PubMed ID: 10181716
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.