BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

682 related articles for article (PubMed ID: 11706859)

  • 41. Medical devices; substantial equivalence; 510(K) summaries and 510(K) statements; class III summaries; confidentiality of information--FDA. Final rule.
    Fed Regist; 1994 Dec; 59(239):64287-96. PubMed ID: 10139433
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Gastroenterology and urology devices; effective date of requirement for premarket approval of the implanted mechanical/hydraulic urinary continence device. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Sep; 65(187):57726-32. PubMed ID: 11503643
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cardiovascular devices; reclassification of certain percutaneous transluminal coronary angioplasty (PTCA) catheters. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2010 Sep; 75(173):54493-6. PubMed ID: 20824947
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Medical Devices; hematology and pathology devices; reclassification of automated blood cell separator device operating by filtration principle from class III to class II. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Feb; 68(40):9530-2. PubMed ID: 12617085
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Medical devices; reclassification of the cutaneous carbon dioxide and the cutaneous oxygen monitor. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Dec; 67(240):76678-81. PubMed ID: 12481766
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Gastroenterology-urology devices; effective date of requirement for premarket approval of the penile inflatable implant. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr; 65(71):19650-8. PubMed ID: 11010632
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Medical devices; immunology and microbiology devices; classification of the West Nile Virus IgM capture Elisa assay. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Oct; 68(210):61743-5. PubMed ID: 14587527
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Medical devices; reclassification of three anesthesiology preamendments class III devices into class II. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2001 Nov; 66(221):57366-8. PubMed ID: 11776278
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Medical devices; reclassification of six cardiovascular preamendments class III devices into class II. Final rule.
    Food and Drug Administration
    Fed Regist; 2001 Apr; 66(69):18540-2. PubMed ID: 11721689
    [TBL] [Abstract][Full Text] [Related]  

  • 51. General hospital and personal use devices: proposed classification of liquid chemical sterilants and general purpose disinfectants--FDA. Proposed rule.
    Fed Regist; 1998 Nov; 63(215):59917-21. PubMed ID: 10187388
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Dental devices; effective date of requirement for premarket approval; temporomandibular joint prostheses--FDA. Final rule.
    Fed Regist; 1998 Dec; 63(250):71743-6. PubMed ID: 10339055
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Dental devices; classification for intraoral devices for snoring and/or obstructive sleep apnea. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Nov; 67(218):68510-2. PubMed ID: 12428642
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Medical devices; neurological devices; classification of cranial orthosis--FDA. Final rule.
    Fed Regist; 1998 Jul; 63(146):40650-2. PubMed ID: 10181519
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Medical devices; immunology and microbiology devices; classification of AFP-L3% immunological test systems. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2005 Oct; 70(191):57748-50. PubMed ID: 16206426
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Dental devices; dental noble metal alloys and dental base metal alloys; designation of special controls. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2004 Aug; 69(162):51765-6. PubMed ID: 15329980
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, and distributor reporting--FDA. Direct final rule.
    Fed Regist; 1998 May; 63(91):26069-77. PubMed ID: 10179334
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Medical devices; gastroenterology and urology devices; classification of the electrogastrography system. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Sep; 64(184):51442-4. PubMed ID: 11010709
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 35.