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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

315 related items for PubMed ID: 10179874

  • 1.
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  • 2. Medical devices; exemption from premarket notification and reserved devices; class I. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan 14; 65(10):2296-323. PubMed ID: 11010655
    [Abstract] [Full Text] [Related]

  • 3. Agency information collection activities; announcement of OMB approval; medical devices: third-party review program under the U.S./EC MRA. Food and Drug Administration, HHS. Notice.
    Fed Regist; 1999 Mar 08; 64(44):11018. PubMed ID: 10557621
    [Abstract] [Full Text] [Related]

  • 4. Medical devices; exemption from premarket notification and reserved devices; Class I--FDA. Proposed rule.
    Fed Regist; 1998 Nov 12; 63(218):63222-53. PubMed ID: 10187398
    [Abstract] [Full Text] [Related]

  • 5. Medical devices; device tracking; new orders to manufacturers--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10638-40. PubMed ID: 10177504
    [Abstract] [Full Text] [Related]

  • 6. Medical devices; exemptions from premarket notification and reserved devices; class I--FDA. Notice.
    Fed Regist; 1998 Feb 02; 63(21):5387-93. PubMed ID: 10177333
    [Abstract] [Full Text] [Related]

  • 7. FDA modernization act of 1997: guidance on medical device tracking; availability--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10640-1. PubMed ID: 10177505
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  • 9. Medical devices; exemptions from premarket notification; class II devices--FDA, Final rule.
    Fed Regist; 1998 Nov 03; 63(212):59222-31. PubMed ID: 10187384
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Medical devices; humanitarian use of devices; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr 17; 63(74):19196-200. PubMed ID: 10178431
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Medical devices; humanitarian use of devices--FDA. Direct final rule.
    Fed Regist; 1998 Apr 17; 63(74):19185-90. PubMed ID: 10178430
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  • 15. Medical devices; exemptions from premarket notification; class II devices; vascular tunnelers. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Mar 03; 65(43):11466-7. PubMed ID: 11010650
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  • 18. 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
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  • 20. 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 22; 65(226):70305-7. PubMed ID: 11503713
    [Abstract] [Full Text] [Related]

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