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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

354 related items for PubMed ID: 10171013

  • 21. 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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  • 22. AHA objects to key parts of device regulations.
    DePorter J.
    Health Facil Manage; 1992 Apr 27; 5(4):38, 40, 42 passim. PubMed ID: 10116728
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  • 26. 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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  • 29. Amended economic impact analysis of final rule requiring use of labeling on natural rubber containing devices--FDA. Final rule; amended economic analysis statement.
    Fed Regist; 1998 Aug 31; 63(168):46171-4. PubMed ID: 10182698
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  • 30. 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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  • 32. Investigational new drug applications; clinical holds; companion document to direct final rule--FDA. Proposed rule.
    Fed Regist; 1998 Dec 14; 63(239):68710-2. PubMed ID: 10187560
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  • 33. Dental devices; effective date of requirement for premarket approval; temporomandibular joint prostheses--FDA. Final rule.
    Fed Regist; 1998 Dec 30; 63(250):71743-6. PubMed ID: 10339055
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  • 34. Amended economic impact analysis of final rule requiring use of labeling on natural rubber containing devices--FDA. Final rule; amended economic analysis statement.
    Fed Regist; 1998 Jun 01; 63(104):29552-90. PubMed ID: 10179863
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  • 36. Dental devices; classification for intraoral devices for snoring and/or obstructive sleep apnea. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Nov 12; 67(218):68510-2. PubMed ID: 12428642
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  • 37. Medical devices; procedures for premarket notification, premarket approval, classification, performance standards establishment, banning devices, and availability of regulatory hearings--FDA. Final rule.
    Fed Regist; 1992 Dec 10; 57(238):58400-6. PubMed ID: 10123143
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