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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

293 related items for PubMed ID: 21121182

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  • 3. Medical devices; hearing aids; technical data amendments. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2008 Jun 02; 73(106):31358-60. PubMed ID: 18677822
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  • 4. 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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  • 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. 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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  • 9. 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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  • 11. 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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  • 13. Removal of regulations regarding certification of drugs composed wholly or partly of insulin--FDA. Direct final rule.
    Fed Regist; 1998 May 13; 63(92):26694-9. PubMed ID: 10179341
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  • 14. Medical devices; reprocessed single-use devices; requirement for submission of validation data. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Sep 25; 71(185):55729-37. PubMed ID: 17017469
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  • 15. 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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  • 18. Amendment to the current good manufacturing practice regulations for finished pharmaceuticals. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Dec 04; 72(232):68064-70. PubMed ID: 18064770
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  • 19. 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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  • 20. Revision to requirements for licensed Anti-Human Globulin and Blood Grouping Reagents. Food and Drug Administration, HHS. Direct final rule.
    Fed Regist; 2000 Dec 12; 65(239):77497-9. PubMed ID: 11503726
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