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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

513 related items for PubMed ID: 10181725

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  • 6. 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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  • 7. 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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  • 8. 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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  • 9. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Apr 27; 63(80 Pt 1):20558-61. PubMed ID: 10179320
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  • 10. 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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  • 12. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Direct final rule; withdrawal.
    Fed Regist; 1998 Aug 11; 63(154):42699. PubMed ID: 10182563
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  • 13. 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
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  • 14. Medical devices; medical device reporting. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2005 Feb 28; 70(38):9516-28. PubMed ID: 15736310
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  • 15. Amendment of various device regulations to reflect current American Society for Testing and Material citations. Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 2000 Jan 24; 65(15):3584-5. PubMed ID: 11010654
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  • 16. Investigational new drug applications; clinical holds--FDA. Direct final rule.
    Fed Regist; 1998 Dec 14; 63(239):68676-8. PubMed ID: 10187558
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  • 19. Amendment to examination and investigation sample requirements--FDA. Direct final rule.
    Fed Regist; 1998 Sep 25; 63(186):51297-9. PubMed ID: 10185810
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  • 20. Quality mammography standards. Department of Health and Human Services (HHS), Public Health Service (PHS), Food and Drug Administration (FDA). Direct final rule.
    Fed Regist; 1999 Jun 17; 64(116):32404-7. PubMed ID: 10558582
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