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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

350 related items for PubMed ID: 10180297

  • 1. Guidance of FDA's expectations of medical device manufacturers concerning the year 2000 date problem--FDA. Notice.
    Fed Regist; 1998 Jun 24; 63(121):34433-42. PubMed ID: 10180297
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  • 3. 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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  • 5. FDA Modernization Act of 1997: modifications to the list of recognized standards; availability; withdrawal of draft guidance "Use of IEC 60601 standards; medical electrical equipment"--FDA. Notice.
    Fed Regist; 1998 Oct 16; 63(200):55617-30. PubMed ID: 10185835
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  • 9. Medical devices; reconditioners, rebuilders of medical devices; revocation of compliance policy guide; request for comments--FDA. Notice.
    Fed Regist; 1998 Dec 04; 63(233):67076-8. PubMed ID: 10338883
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  • 10. Medical devices; medical device reporting; baseline reports. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jun 13; 73(115):33692-5. PubMed ID: 18677824
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  • 11. Draft guidance for industry; exports and imports under the FDA Export Reform and Enhancement Act of 1996--FDA. Notice.
    Fed Regist; 1998 Jun 12; 63(113):32219-34. PubMed ID: 10180275
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  • 14. Medical devices: reports of corrections and removals; delay of effective data--FDA. Direct final rule; delay of effective date.
    Fed Regist; 1998 Nov 18; 63(222):63983. PubMed ID: 10339047
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  • 15. 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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  • 18. Letter to manufacturers of blood establishment computer software products--FDA. Notice.
    Fed Regist; 1994 Aug 31; 59(168):44991-2. PubMed ID: 10136917
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  • 19. FDA weighs policing electronic patient record.
    Hosp Case Manag; 1997 May 31; 5(5):81-3. PubMed ID: 10167258
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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
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