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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

253 related items for PubMed ID: 10557621

  • 1. Agency information collection activities; announcement of OMB approval; medical devices: third-party review program under the U.S./EC MRA. Food and Drug Administration, HHS. Notice.
    Fed Regist; 1999 Mar 08; 64(44):11018. PubMed ID: 10557621
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  • 4. Medical devices; reports of corrections and removals; lift of stay of effective date--FDA. Final rule; lift of stay of effective date.
    Fed Regist; 1998 Apr 16; 63(73):18836. PubMed ID: 10179315
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  • 7. 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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  • 8. Medical devices; exemption from premarket notification and reserved devices; class I. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Jan 14; 65(10):2296-323. PubMed ID: 11010655
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  • 11. Medical devices; gastroenterology-urology devices; nonimplanted, peripheral electrical continence device. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 07; 65(68):18236-7. PubMed ID: 11010624
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  • 12. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices), guidance for FDA reviewers and industry; availability--FDA. Notice.
    Fed Regist; 1998 Nov 06; 63(215):60009-10. PubMed ID: 10187389
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  • 13. Draft guidance for industry; exports and imports under the FDA Export Reform and Enhancement Act of 1996--FDA.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. FDA Modernization Act of 1997: modifications to the list of recognized standards; availability; withdrawal of draft guidance "Use of IEC 60601 standards; medical electrical equipment"--FDA.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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  • 15. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Final rule.
    Fed Regist; 1998 Oct 08; 63(195):54042-4. PubMed ID: 10185825
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  • 16. Approval of an alternative requirement of the Mammography Quality Standards Act; availability--FDA. Notice.
    Fed Regist; 1998 Nov 09; 63(216 Pt 1):60352. PubMed ID: 10187394
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  • 17. Clinical chemistry and clinical toxicology devices; classification of B-type natriuretic peptide test system. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2001 Feb 28; 66(40):12733-4. PubMed ID: 11503864
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  • 18. Medical devices; reclassification and codification of the stainless steel suture. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 13; 65(72):19835-6. PubMed ID: 11010635
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  • 19. Medtronic, Inc.; premarket approval of the Interstim Sacral Nerve Stimulation (SNS) System--FDA. Notice.
    Fed Regist; 1998 Jan 29; 63(19):4457. PubMed ID: 10177327
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