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PUBMED FOR HANDHELDS

Journal Abstract Search

1028 related items for PubMed ID: 17138391

  • 1. FDA marketing claims, and the practitioner.
    Runner S.
    J Evid Based Dent Pract; 2006 Mar; 6(1):19-23. PubMed ID: 17138391
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  • 3. Medical devices; device tracking--FDA. Final rule; suspension of effective date; notification of status under the Safe Medical Devices Act; technical amendments.
    Fed Regist; 1993 Aug 16; 58(156):43442-51. PubMed ID: 10127886
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  • 6. Medical devices; reclassification of six cardiovascular preamendments class III devices into class II. Final rule.
    Food and Drug Administration.
    Fed Regist; 2001 Apr 10; 66(69):18540-2. PubMed ID: 11721689
    [Abstract] [Full Text] [Related]

  • 7. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
    Alder HC.
    Hosp Technol Ser; 1993 Oct 10; 12(11):1-27. PubMed ID: 10129209
    [Abstract] [Full Text] [Related]

  • 8. Medical device recall authority--FDA. Final rule.
    Fed Regist; 1996 Nov 20; 61(225):59004-22. PubMed ID: 10163116
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  • 10. Cochlear implants: overview of safety and effectiveness. The FDA evaluation.
    Yin L, Segerson DA.
    Otolaryngol Clin North Am; 1986 May 20; 19(2):423-33. PubMed ID: 3520445
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  • 13. 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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  • 14. What physicians should know about the regulation of Obstetric and Gynecologic Medical Devices.
    Yin L.
    J Reprod Med; 1983 Jan 04; 28(1):3-11. PubMed ID: 6834344
    [Abstract] [Full Text] [Related]

  • 15. Medical devices; neurological devices; classification of cranial orthosis--FDA. Final rule.
    Fed Regist; 1998 Jul 30; 63(146):40650-2. PubMed ID: 10181519
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  • 16. Medical devices; device tracking; new orders to manufacturers--FDA. Notice.
    Fed Regist; 1998 Mar 04; 63(42):10638-40. PubMed ID: 10177504
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  • 18. Medical devices; reports of corrections and removals; companion to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Aug 07; 63(152):42300-4. PubMed ID: 10181727
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  • 20. 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]

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