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PUBMED FOR HANDHELDS

Journal Abstract Search


129 related items for PubMed ID: 12026712

  • 1.
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  • 2. 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
    [Abstract] [Full Text] [Related]

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  • 4. Sacral nerve stimulation for urinary control.
    Clin Privil White Pap; 2005 Mar 30; (227):1-8. PubMed ID: 15742527
    [No Abstract] [Full Text] [Related]

  • 5. FDA approves first wearable defibrillator.
    FDA Consum; 2002 Mar 30; 36(2):3. PubMed ID: 11989468
    [No Abstract] [Full Text] [Related]

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  • 7. Electrical anesthesia.
    Quarnstrom FC.
    J Calif Dent Assoc; 1988 Dec 30; 16(12):35-40. PubMed ID: 2482869
    [No Abstract] [Full Text] [Related]

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  • 9. FDA notifications. FC2 female condom receives FDA approval.
    AIDS Alert; 2009 May 30; 24(5):58-9. PubMed ID: 19455720
    [No Abstract] [Full Text] [Related]

  • 10. A transcutaneous electrical nerve stimulation device (Cefaly) for migraine prevention.
    Med Lett Drugs Ther; 2014 Aug 18; 56(1449):78. PubMed ID: 25118802
    [No Abstract] [Full Text] [Related]

  • 11. [Transcutaneous neural stimulation as a therapeutic method for use in pain disorders and dysfunctions of the stomatognathic system].
    Teseo Mainieri E.
    RGO; 1983 Aug 18; 31(3):270-2. PubMed ID: 6333055
    [No Abstract] [Full Text] [Related]

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  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. FDA clears pocket-sized electrocardiograph.
    FDA Consum; 2002 Dec 02; 36(3):5. PubMed ID: 12085817
    [No Abstract] [Full Text] [Related]

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  • 17. FDA perspective on clinical trial design for cardiovascular devices.
    Chen E, Sapirstein W, Ahn C, Swain J, Zuckerman B.
    Ann Thorac Surg; 2006 Sep 02; 82(3):773-5. PubMed ID: 16928481
    [No Abstract] [Full Text] [Related]

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  • 19. 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]

  • 20. Orthopedic devices; effective data of requirement for premarket approval for hip joint metal/polymer or ceramic/polymer semiconstrained resurfacing cemented prosthesis. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2004 Oct 04; 69(191):59132-4. PubMed ID: 15460583
    [Abstract] [Full Text] [Related]


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