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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

685 related items for PubMed ID: 10177504

  • 21. 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 29; 63(188):51874-5. PubMed ID: 10185813
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  • 22. Medical devices; ear, nose, and throat devices; classification of the transcutaneous air conduction hearing aid system. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Nov 07; 67(216):67789-90. PubMed ID: 12422884
    [Abstract] [Full Text] [Related]

  • 23. Medical devices; obstetrical and gynecological devices; classification of the breast lesion documentation system. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jul 28; 68(144):44413-5. PubMed ID: 12884877
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  • 24. Medical device recall authority--FDA. Final rule.
    Fed Regist; 1996 Nov 20; 61(225):59004-22. PubMed ID: 10163116
    [Abstract] [Full Text] [Related]

  • 25. Export of pharmaceuticals and medical devices under the federal Food, Drug & Cosmetic Act: FDA's striking change in interpretation post-Shelhigh.
    Basile EM, Tolomeo D, Gluck E.
    Food Drug Law J; 2009 Nov 20; 64(1):149-69. PubMed ID: 19998744
    [Abstract] [Full Text] [Related]

  • 26. Medical devices; refurbishers, rebuilders, reconditioners, servicers, and "as is" remarketers of medical devices; review and revision of compliance policy guides and regulatory requirements; request for comments and information--FDA. Advance notice of proposed rulemaking.
    Fed Regist; 1997 Dec 23; 62(246):67011-3. PubMed ID: 10179309
    [Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. Medical devices; humanitarian use of devices--FDA. Final rule.
    Fed Regist; 1998 Nov 03; 63(212):59217-22. PubMed ID: 10187383
    [Abstract] [Full Text] [Related]

  • 29. 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]

  • 30. 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]

  • 31. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review--FDA. Direct final rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20530-3. PubMed ID: 10179319
    [Abstract] [Full Text] [Related]

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  • 35. 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
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  • 39. 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
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