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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

306 related items for PubMed ID: 10178431

  • 21. Medical device reporting: manufacturer reporting, importer reporting, user facility reporting, distributor reporting. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan 26; 65(17):4112-21. PubMed ID: 11010653
    [Abstract] [Full Text] [Related]

  • 22. Administrative practices and procedures; internal agency review of decisions; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Jun 16; 63(115):32772-4. PubMed ID: 10180279
    [Abstract] [Full Text] [Related]

  • 23. Medical devices; immunology and microbiology devices; classification of the endotoxin assay. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Oct 31; 68(211):62007-8. PubMed ID: 14594019
    [Abstract] [Full Text] [Related]

  • 24. Medical devices; immunology and microbiology devices; classification of the immunomagnetic circulating cancer cell selection and enumeration system. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 May 11; 69(91):26036-8. PubMed ID: 15137395
    [Abstract] [Full Text] [Related]

  • 25. 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 07; 68(129):40125-7. PubMed ID: 12858842
    [Abstract] [Full Text] [Related]

  • 26. General hospital and personal use devices; classification of the Apgar timer, lice removal kit, and infusion stand--FDA. Proposed rule.
    Fed Regist; 1998 Mar 10; 63(46):11632-3. PubMed ID: 10177746
    [Abstract] [Full Text] [Related]

  • 27. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Final rule.
    Fed Regist; 1998 Oct 08; 63(195):54042-4. PubMed ID: 10185825
    [Abstract] [Full Text] [Related]

  • 28. Removal of regulations regarding certification of drugs composed wholly or partly of insulin--FDA. Direct final rule.
    Fed Regist; 1998 May 13; 63(92):26694-9. PubMed ID: 10179341
    [Abstract] [Full Text] [Related]

  • 29. 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 07; 70(214):67353-5. PubMed ID: 16273747
    [Abstract] [Full Text] [Related]

  • 30. Investigational new drug applications; clinical holds; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Dec 14; 63(239):68710-2. PubMed ID: 10187560
    [Abstract] [Full Text] [Related]

  • 31. Medical devices; investigational device exemptions--FDA. Proposed rule.
    Fed Regist; 1998 Jul 15; 63(135):38131-8. PubMed ID: 10181246
    [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 30; 68(210):61743-5. PubMed ID: 14587527
    [Abstract] [Full Text] [Related]

  • 33. Medical devices; ear, nose and throat devices; reclassification of the endolymphatic shunt tube with valve. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Apr 29; 67(82):20893-4. PubMed ID: 11980454
    [Abstract] [Full Text] [Related]

  • 34. Medical devices: cardiovascular devices: reclassification of the arrhythmia detector and alarm. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Oct 28; 68(208):61342-4. PubMed ID: 14584507
    [Abstract] [Full Text] [Related]

  • 35. Dental devices; classification for intraoral devices for snoring and/or obstructive sleep apnea. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Nov 12; 67(218):68510-2. PubMed ID: 12428642
    [Abstract] [Full Text] [Related]

  • 36. Orthopedic devices: classification and reclassification of pedicle screw spinal systems--FDA. Final rule.
    Fed Regist; 1998 Jul 27; 63(143):40025-41. PubMed ID: 10181517
    [Abstract] [Full Text] [Related]

  • 37. 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 16; 69(51):12271-3. PubMed ID: 15025053
    [Abstract] [Full Text] [Related]

  • 38. Medical devices; immunology and microbiology devices; classification of the beta-glucan serological assay. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Sep 23; 69(184):56934-6. PubMed ID: 15386877
    [Abstract] [Full Text] [Related]

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  • 40. 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 22; 66(99):28051-3. PubMed ID: 11712575
    [Abstract] [Full Text] [Related]

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