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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

388 related items for PubMed ID: 10339055

  • 21. 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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  • 24. Medical devices: classification of the dental sonography device and jaw tracking device. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Dec 02; 68(231):67365-7. PubMed ID: 14651050
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  • 27. 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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  • 28. Medical devices; investigational device exemptions--FDA. Final rule.
    Fed Regist; 1998 Nov 23; 63(225):64617-26. PubMed ID: 10338870
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  • 30. Medical devices; reclassification and codification of suction lipoplasty system for aesthetic body contouring--FDA. Final rule.
    Fed Regist; 1998 Feb 17; 63(31):7703-5. PubMed ID: 10177951
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  • 33. Medical devices; effective date of requirement for premarket approval for three class III preamendments physical medicine devices--FDA. Proposed rule; opportunity to request a change in classification.
    Fed Regist; 1998 Jul 30; 63(146):40677-81. PubMed ID: 10181521
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  • 34. Effective date of requirement for premarket approval for a pacemaker programmer. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2012 Jun 22; 77(121):37570-3. PubMed ID: 22730574
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  • 35. Medical devices; reclassification of the cutaneous carbon dioxide and the cutaneous oxygen monitor. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2002 Dec 13; 67(240):76678-81. PubMed ID: 12481766
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  • 36. Medical devices; exemptions from premarket notification and reserved devices; class I--FDA. Notice.
    Fed Regist; 1998 Feb 02; 63(21):5387-93. PubMed ID: 10177333
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  • 38. Effective date of requirement for premarket approval for cardiovascular permanent pacemaker electrode. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2012 Jul 06; 77(130):39924-7. PubMed ID: 22792583
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  • 40. Ear, nose, and throat devices; classification of the nasal dilator, the intranasal splint, and the bone particle collector. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 1999 Mar 08; 64(44):10947-9. PubMed ID: 10557619
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