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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

429 related items for PubMed ID: 16226095

  • 1. Use of standards in the review of medical devices.
    Ho C, Jensen D, Lacy F, Muni N, Reilly S, Mallis E.
    J Electrocardiol; 2005 Oct; 38(4 Suppl):171-4. PubMed ID: 16226095
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  • 3. Safe Medical Devices Act: management guidance for hospital compliance with the new FDA requirements.
    Alder HC.
    Hosp Technol Ser; 1993 Oct; 12(11):1-27. PubMed ID: 10129209
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  • 4. Medical devices; exemption from premarket notification requirements; class I devices; technical amendment. Final rule; technical amendment.
    Food and Drug Administration. HHS.
    Fed Regist; 2001 Jul 25; 66(143):38786-819. PubMed ID: 11725800
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  • 5. 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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  • 7. Standards for humidification and filtration devices.
    Stevens J.
    Respir Care Clin N Am; 2006 Jun 14; 12(2):203-32. PubMed ID: 16828691
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  • 8. Medical devices: the obvious, the readily-accepted, and the surprising.
    Tolomeo DE, Clarke LA.
    J Health Life Sci Law; 2008 Jul 14; 1(4):117, 119-44. PubMed ID: 18717154
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  • 12. Public information; communications with state and foreign government officials--FDA. Proposed rule.
    Fed Regist; 1998 Jul 27; 63(143):40069-72. PubMed ID: 10181518
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  • 13. An overview of FDA medical device regulation as it relates to deep brain stimulation devices.
    Peña C, Bowsher K, Costello A, De Luca R, Doll S, Li K, Schroeder M, Stevens T.
    IEEE Trans Neural Syst Rehabil Eng; 2007 Sep 27; 15(3):421-4. PubMed ID: 17894274
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  • 14. 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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  • 18. Health device legislation: an overview of the law and its impact on respiratory care.
    Bancroft ML, Steen JA.
    Respir Care; 1978 Dec 06; 23(12):1179-84. PubMed ID: 10315033
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  • 20. Dissemination of information on unapproved/new uses for marketed drugs, biologics, and devices--FDA. Proposed rule.
    Fed Regist; 1998 Jun 08; 63(109):31143-61. PubMed ID: 10180130
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