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 *

602 related articles for article (PubMed ID: 10127886)

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

  • 22. Medical devices: reports of corrections and removals; delay of effective data--FDA. Direct final rule; delay of effective date.
    Fed Regist; 1998 Nov; 63(222):63983. PubMed ID: 10339047
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review--FDA. Direct final rule.
    Fed Regist; 1998 Apr; 63(80 Pt 1):20530-3. PubMed ID: 10179319
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Medical devices; immunology and microbiology devices; classification of the endotoxin assay. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Oct; 68(211):62007-8. PubMed ID: 14594019
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Aug; 63(154):42699. PubMed ID: 10182563
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Medical devices; humanitarian use of devices--FDA. Direct final rule.
    Fed Regist; 1998 Apr; 63(74):19185-90. PubMed ID: 10178430
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Medical devices; establishment registration and device listing for manufacturers and distributors of devices; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Sep; 63(188):51874-5. PubMed ID: 10185813
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Computerized medical device tracking--ways to comply with SMDA (Safe Medical Devices Act of 1990).
    Landis D
    Healthc Inform; 1992 Jul; 9(7):36, 38, 40-2. PubMed ID: 10119858
    [No Abstract]   [Full Text] [Related]  

  • 30. Medical devices; classification for medical washer and medical washer-disinfector. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Nov; 67(221):69119-21. PubMed ID: 12437015
    [TBL] [Abstract][Full Text] [Related]  

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

  • 32. Medical devices; clinical chemistry and clinical toxicology devices; classification of the breath nitric oxide test system. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Jul; 68(129):40125-7. PubMed ID: 12858842
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Orthopedic devices: classification and reclassification of pedicle screw spinal systems; technical amendment. Final rule; technical amendment.
    Food and Drug Administration, HHS
    Fed Regist; 2001 May; 66(99):28051-3. PubMed ID: 11712575
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Medical devices; preemption of state product liability claims--FDA. Withdrawal of proposed rule.
    Fed Regist; 1998 Jul; 63(142):39789-90. PubMed ID: 10181516
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Medical devices: classification of the dental sonography device and jaw tracking device. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Dec; 68(231):67365-7. PubMed ID: 14651050
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cardiovascular and neurological devices; reclassification of two embolization devices. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2004 Dec; 69(249):77898-900. PubMed ID: 15624254
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Safe Medical Devices Act of 1990--FDA. Notice.
    Fed Regist; 1991 Apr; 56(66):14111-3. PubMed ID: 10111151
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Medical devices; exemption from premarket notification requirements; class I devices; technical amendment. Final rule; technical amendment.
    Food and Drug Administration. HHS
    Fed Regist; 2001 Jul; 66(143):38786-819. PubMed ID: 11725800
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Medical devices; humanitarian use of devices; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr; 63(74):19196-200. PubMed ID: 10178431
    [TBL] [Abstract][Full Text] [Related]  

  • 40. General and plastic surgery devices; classification of silicone sheeting. Final rule.
    Food and Drug Administration. HHS
    Fed Regist; 2004 Aug; 69(152):48146-8. PubMed ID: 15300956
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 31.