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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

285 related items for PubMed ID: 10179309

  • 1. 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
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  • 2. Medical devices; review and revision of compliance policy guides and regulatory requirements for refurbishers, rebuilders, reconditioners, servicers and "as is" remarketers of medical devices; request for comments and information; extension of comment period--FDA. Advance notice of proposed rulemaking; extension of comment period.
    Fed Regist; 1998 Mar 25; 63(57):14390-1. PubMed ID: 10177751
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  • 5. Diagnostic x-ray equipment performance standard; request for comments and information--FDA. Advance notice of proposed rulemaking.
    Fed Regist; 1997 Dec 11; 62(238):65235-7. PubMed ID: 10176581
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  • 7. 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
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  • 8. 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
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  • 9. Medical devices; device tracking--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
    Fed Regist; 1992 May 29; 57(104):22966-70. PubMed ID: 10171013
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  • 10. 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
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  • 11. 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
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  • 12. Administrative practices and procedures; internal review of agency decisions---FDA. Direct final rule.
    Fed Regist; 1998 Jun 16; 63(115):32733-5. PubMed ID: 10180278
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  • 13. Medical devices; effective date of requirement for premarket approval for three class III preamendments devices--FDA. Proposed rule; opportunity to request a change in classification.
    Fed Regist; 1998 Aug 18; 63(159):44177-81. PubMed ID: 10184983
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  • 14. Medical devices; implementation of third party review under the Food and Drug Administration Modernization Act of 1997; emergency processing request under OMB review--FDA. Notice.
    Fed Regist; 1998 May 22; 63(99):28388-91. PubMed ID: 10179874
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  • 15. 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 May 22; 64(1):149-69. PubMed ID: 19998744
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  • 17. Medical devices; establishment registration and device listing for manufacturers and distributors of devices--FDA. Direct final rule.
    Fed Regist; 1998 Sep 29; 63(188):51825-7. PubMed ID: 10185812
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  • 19. Medical devices; investigational device exemptions--FDA. Proposed rule.
    Fed Regist; 1998 Jul 15; 63(135):38131-8. PubMed ID: 10181246
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  • 20. 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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