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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

259 related items for PubMed ID: 23476999

  • 21. Medical devices; effective date of requirement for premarket approval for three preamendment class III devices. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 13; 65(72):19833-4. PubMed ID: 11010634
    [Abstract] [Full Text] [Related]

  • 22. Gastroenterology-urology devices; effective date of requirement for premarket approval of the penile inflatable implant. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Apr 12; 65(71):19650-8. PubMed ID: 11010632
    [Abstract] [Full Text] [Related]

  • 23. Medical devices; obstetrical and gynecological devices; classification of the breast lesion documentation system. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Jul 28; 68(144):44413-5. PubMed ID: 12884877
    [Abstract] [Full Text] [Related]

  • 24. Medical devices; ophthalmic devices; classification of the scleral plug. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2013 Nov 15; 78(221):68714-5. PubMed ID: 24236336
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  • 26. 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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  • 31. Medical Devices; Exemption From Premarket Notification: Method, Metallic Reduction, Glucose (Urinary, Nonquantitative) Test System in a Reagent Tablet Format. Final order.
    Food and Drug Administration, HHS.
    Fed Regist; 2016 Oct 04; 81(192):68293-5. PubMed ID: 27731614
    [Abstract] [Full Text] [Related]

  • 32. Medical Devices; Exemption From Premarket Notification; Method, Metallic Reduction, Glucose (Urinary, Nonquantitative) Test System in a Reagent Tablet Format. Final order.
    Food and Drug Administration, HHS.
    Fed Regist; 2016 Oct 04; 81(192):68295-7. PubMed ID: 27731615
    [Abstract] [Full Text] [Related]

  • 33. Cardiovascular devices; reclassification of external counter-pulsating devices for treatment of chronic stable angina; effective date of requirement for premarket approval for external counter-pulsating devices for other specified intended uses. Final order.
    Food and Drug Administration, HHS.
    Fed Regist; 2013 Dec 30; 78(250):79304-8. PubMed ID: 24383148
    [Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35. Cardiovascular devices; reclassification of certain percutaneous transluminal coronary angioplasty (PTCA) catheters. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2010 Sep 08; 75(173):54493-6. PubMed ID: 20824947
    [Abstract] [Full Text] [Related]

  • 36. Medical devices; effective date of requirement for premarket approval for three class III preamendments devices--FDA. Proposed rule; opportunity to request a change in classification.
    Fed Regist; 1998 Aug 18; 63(159):44177-81. PubMed ID: 10184983
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  • 37. Gastroenterology-urology devices; reclassification of implanted blood access devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2014 Jul 25; 79(143):43241-6. PubMed ID: 25118367
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  • 39. Medical devices; hematology and pathology devices; classification of the Factor V Leiden DNA mutation detection systems devices. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Mar 16; 69(51):12271-3. PubMed ID: 15025053
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