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 *

350 related articles for article (PubMed ID: 12751500)

  • 21. Medical devices; medical device reporting; baseline reports. Direct final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2008 Jun; 73(115):33692-5. PubMed ID: 18677824
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Off-label use of medical devices in radiology: regulatory standards and recent developments.
    Smith JJ
    J Am Coll Radiol; 2010; 7(2):115-9. PubMed ID: 20142085
    [TBL] [Abstract][Full Text] [Related]  

  • 23. FDA approves only 1 HIV home test kit.
    AIDS Read; 2008 May; 18(5):236. PubMed ID: 18589478
    [No Abstract]   [Full Text] [Related]  

  • 24. Medical devices; effective date of requirement for premarket approval for three class III preamendments physical medicine devices--FDA. Proposed rule; opportunity to request a change in classification.
    Fed Regist; 1998 Jul; 63(146):40677-81. PubMed ID: 10181521
    [TBL] [Abstract][Full Text] [Related]  

  • 25. General hospital and personal use devices; premarket approval of the infant radiant warmer--FDA. Proposed rule.
    Fed Regist; 1986 Jan; 51(10):1910-5. PubMed ID: 10275304
    [TBL] [Abstract][Full Text] [Related]  

  • 26. FDA approves new HIV blood test from Roche.
    AIDS Read; 2009 Mar; 19(3):123. PubMed ID: 19338065
    [No Abstract]   [Full Text] [Related]  

  • 27. US FDA perspective on the regulations of medical-grade polymers: cyanoacrylate polymer medical device tissue adhesives.
    Mattamal GJ
    Expert Rev Med Devices; 2008 Jan; 5(1):41-9. PubMed ID: 18095895
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The FDA may not regulate tobacco products as "drugs" or as "medical devices".
    Merrill RA
    Duke Law J; 1998 Apr; 47(6):1071-94. PubMed ID: 10557545
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Orthopedic devices; effective data of requirement for premarket approval for hip joint metal/polymer or ceramic/polymer semiconstrained resurfacing cemented prosthesis. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2004 Oct; 69(191):59132-4. PubMed ID: 15460583
    [TBL] [Abstract][Full Text] [Related]  

  • 30. FDA & digital mammography: why has FDA required full field digital mammography systems to be regulated as potentially dangerous devices for more than 10 years?
    Nields MW
    Acad Radiol; 2010 May; 17(5):652-7. PubMed ID: 20380981
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Medical devices; hematology and pathology devices; classification of the Factor V Leiden DNA mutation detection systems devices. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2004 Mar; 69(51):12271-3. PubMed ID: 15025053
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Guidance for the emergency use of unapproved medical devices; availability--FDA. Notice.
    Fed Regist; 1985 Oct; 50(204):42866-7. PubMed ID: 10274027
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Strategic planning for U.S. premarket approval submissions.
    Donawa M
    Med Device Technol; 2006 Sep; 17(7):21-3. PubMed ID: 17039953
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Regulatory aspects of invasive glucose measurements.
    Gutman S; Bernhardt P; Pinkos A; Moxey-Mims M; Knott T; Cooper J
    Diabetes Technol Ther; 2002; 4(6):775-7. PubMed ID: 12685800
    [TBL] [Abstract][Full Text] [Related]  

  • 35. How do Orthopaedic Devices Change After Their Initial FDA Premarket Approval?
    Samuel AM; Rathi VK; Grauer JN; Ross JS
    Clin Orthop Relat Res; 2016 Apr; 474(4):1053-68. PubMed ID: 26584802
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Home test kit approved; marketing to begin shortly.
    AIDS Policy Law; 1996 May; 11(10):1, 8. PubMed ID: 11363491
    [TBL] [Abstract][Full Text] [Related]  

  • 37. New obstacles in the path of marketing new medical devices.
    Bucci VA; Reiss JB; Hall NC
    J Health Care Technol; 1985; 2(2):81-96. PubMed ID: 10300491
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Good gene hunting: commercializing safety and efficacy of home genetic test kits.
    Stevenson M
    J Biolaw Bus; 1999; 3(1):29-39. PubMed ID: 11933969
    [TBL] [Abstract][Full Text] [Related]  

  • 39. FDA weighs policing electronic patient record.
    Hosp Case Manag; 1997 May; 5(5):81-3. PubMed ID: 10167258
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Testing. FDA panel weighs benefits, risks of in-home HIV test.
    AIDS Policy Law; 2005 Nov; 20(21):2. PubMed ID: 16333874
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.