BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

409 related articles for article (PubMed ID: 10181517)

  • 21. Medical devices; gastroenterology-urology devices; classification of the ingestible telemetric gastrointestinal capsule imaging system. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2002 Jan; 67(16):3431-3. PubMed ID: 11820252
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Medical devices: cardiovascular devices: reclassification of the arrhythmia detector and alarm. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Oct; 68(208):61342-4. PubMed ID: 14584507
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Medical devices; general and plastic surgery devices; classification of the low energy ultrasound wound cleaner. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2005 Nov; 70(214):67353-5. PubMed ID: 16273747
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cardiovascular, orthopedic, and physical medicine diagnostic devices; reclassification of cardiopulmonary bypass accessory equipment, goniometer device, and electrode cable devices. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr; 65(70):19317-9. PubMed ID: 11010630
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Immunology and Microbiology Devices; Classification of Anti-Saccharomyces cerevisiae (S. cerevisiae) Antibody (ASCA) Test Systems. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Nov; 65(226):70305-7. PubMed ID: 11503713
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical chemistry and clinical toxicology devices; classification of B-type natriuretic peptide test system. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2001 Feb; 66(40):12733-4. PubMed ID: 11503864
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Orthopedic devices; classification for the resorbable calcium salt bone void filler device. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2003 Jun; 68(105):32635-7. PubMed ID: 12784825
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Medical devices; exemptions from premarket notification; class II devices--FDA, Final rule.
    Fed Regist; 1998 Nov; 63(212):59222-31. PubMed ID: 10187384
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Medical devices; immunology and microbiology devices; classification of the beta-glucan serological assay. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2004 Sep; 69(184):56934-6. PubMed ID: 15386877
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. General hospital and personal use devices; classification of the Apgar timer, lice removal kit, and infusion stand--FDA. Proposed rule.
    Fed Regist; 1998 Mar; 63(46):11632-3. PubMed ID: 10177746
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ear, nose, and throat devices; classification of the nasal dilator, the intranasal splint, and the bone particle collector. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Mar; 64(44):10947-9. PubMed ID: 10557619
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Medical devices; classification/reclassification; restricted devices; analyte specific reagents--FDA. Final rule.
    Fed Regist; 1997 Nov; 62(225):62243-60. PubMed ID: 10177056
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Medical devices; immunology and microbiology devices; classification of reagents for detection of specific novel influenza A viruses. Final rule.
    Food and Drug Administration, HHS
    Fed Regist; 2006 Mar; 71(55):14377-9. PubMed ID: 16562353
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.