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 *

193 related articles for article (PubMed ID: 10248451)

  • 1. Food and Drug Administration--General hospital and personal use devices; general provisions. Final rule.
    Fed Regist; 1980 Oct; 45(205):69678-737. PubMed ID: 10248451
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Medical devices; humanitarian use of devices--FDA. Final rule.
    Fed Regist; 1998 Nov; 63(212):59217-22. PubMed ID: 10187383
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Classification of general hospital and personal use devices; development of general provisions: proposed rule.
    Fed Regist; 1979 Aug; 44(166):49843-54. PubMed ID: 10242812
    [No Abstract]   [Full Text] [Related]  

  • 7. Medical device reporting--FDA. Final rule.
    Fed Regist; 1984 Sep; 49(180):36326-51. PubMed ID: 10267669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Opportunity to request change in classification of continuous ventilator--FDA. Notice; final rule-related.
    Fed Regist; 1983 Jun; 48(118):27723-4. PubMed ID: 10289467
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Medical devices; exemption from premarket notification and reserved devices; class I. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan; 65(10):2296-323. PubMed ID: 11010655
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Medical device reporting--FDA. Reproposal.
    Fed Regist; 1983 May; 48(104):24014-24. PubMed ID: 10261480
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. General and plastic surgery devices; classification of the nonresorbable gauze/sponge for external use, the hydrophilic wound dressing, the occlusive wound dressing, and the hydrogel wound dressing. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Oct; 64(192):53927-9. PubMed ID: 11010701
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.