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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

325 related items for PubMed ID: 19827226

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  • 2. Microbiology devices; reclassification of herpes simplex virus types 1 and 2 serological assays. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2007 Apr 03; 72(63):15828-30. PubMed ID: 17455387
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  • 3. Immunology and microbiology devices; reclassification of the herpes simplex virus serological assay device. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2011 Aug 09; 76(153):48715-7. PubMed ID: 21826824
    [Abstract] [Full Text] [Related]

  • 4. 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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  • 6. Medical devices; reports of corrections and removals--FDA. Direct final rule.
    Fed Regist; 1998 Aug 07; 63(152):42229-33. PubMed ID: 10181725
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  • 10. Microbiology devices; reclassification of hepatitis A virus serological assays. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Feb 09; 71(27):6677-9. PubMed ID: 16502543
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  • 12. Medical devices; pediatric uses of devices; requirement for submission of information on pediatric subpopulations that suffer from a disease or condition that a device is intended to treat, diagnose, or cure; direct final rule. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2010 Apr 01; 75(62):16347-51. PubMed ID: 20383921
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  • 13. 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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  • 14. Revisions to the general safety requirements for biological products--FD. Direct final rule.
    Fed Regist; 1998 Apr 20; 63(75):19399-403. PubMed ID: 10178869
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  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Medical devices; immunology and microbiology devices; classification of reagents for detection of specific novel influenza A viruses. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2006 Mar 22; 71(55):14377-9. PubMed ID: 16562353
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  • 19. Amendments to general regulations of the Food and Drug Administration. Direct final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2010 Nov 30; 75(229):73951-5. PubMed ID: 21121182
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