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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

388 related items for PubMed ID: 20357279

  • 1. Improving the security and privacy of implantable medical devices.
    Maisel WH, Kohno T.
    N Engl J Med; 2010 Apr 01; 362(13):1164-6. PubMed ID: 20357279
    [No Abstract] [Full Text] [Related]

  • 2. Modernizing device regulation.
    Garber AM.
    N Engl J Med; 2010 Apr 01; 362(13):1161-3. PubMed ID: 20335575
    [No Abstract] [Full Text] [Related]

  • 3. Pharmaceuticals and medical devices: medical devices. Issue brief.
    Berry MD.
    Issue Brief Health Policy Track Serv; 2012 Dec 31; ():1-35. PubMed ID: 23297445
    [No Abstract] [Full Text] [Related]

  • 4. Pharmaceuticals and Medical Devices: FDA Oversight.
    White RS, Thomson Reuters Accelus..
    Issue Brief Health Policy Track Serv; 2017 Dec 26; 2017():1-33. PubMed ID: 29361662
    [No Abstract] [Full Text] [Related]

  • 5. Devices and the food and drug administration.
    Phillips SJ, Phillips RS.
    Artif Organs; 2005 May 26; 29(5):363-5. PubMed ID: 15854210
    [No Abstract] [Full Text] [Related]

  • 6. Pharmaceuticals and medical devices: medical devices. End-of-year issue brief.
    Chaps NA.
    Issue Brief Health Policy Track Serv; 2010 Jan 04; ():1-25. PubMed ID: 20217916
    [No Abstract] [Full Text] [Related]

  • 7. Medical devices; exemption from premarket notification and reserved devices; Class I--FDA. Proposed rule.
    Fed Regist; 1998 Nov 12; 63(218):63222-53. PubMed ID: 10187398
    [Abstract] [Full Text] [Related]

  • 8. Pharmaceuticals and Medical Devices: FDA Oversight.
    White RS, Thomson Reuters Accelus..
    Issue Brief Health Policy Track Serv; 2018 Dec 24; 2018():1-42. PubMed ID: 30695853
    [No Abstract] [Full Text] [Related]

  • 9. Combination products regulation at the FDA.
    Lauritsen KJ, Nguyen T.
    Clin Pharmacol Ther; 2009 May 24; 85(5):468-70. PubMed ID: 19381151
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Modernizing device regulation.
    Kretzer RM, Foreman CL, Shuren J.
    N Engl J Med; 2010 Jul 08; 363(2):196-7; author reply 197. PubMed ID: 20653080
    [No Abstract] [Full Text] [Related]

  • 12. Pharmaceuticals and medical devices: medical devices.
    Chaps NA.
    Issue Brief Health Policy Track Serv; 2009 Jan 05; ():1-23. PubMed ID: 19297720
    [No Abstract] [Full Text] [Related]

  • 13. The need for federal preemption of state tort claims in the context of "new drugs" and premarket-approved medical devices.
    Mottes LM.
    Seton Hall Law Rev; 2011 Jan 05; 41(2):723-63. PubMed ID: 21739761
    [No Abstract] [Full Text] [Related]

  • 14. Pharmaceuticals and medical devices: medical devices. Issue brief.
    Health Policy Tracking Service, A Service of Thomson Reuters/West.
    Issue Brief Health Policy Track Serv; 2011 Jan 03; ():1-24. PubMed ID: 21374838
    [No Abstract] [Full Text] [Related]

  • 15. License to maim: federal pre-emption and the Medical Device Amendments of 1976.
    Petrella ME.
    Health Matrix Clevel; 1996 Jan 03; 6(2):349-89. PubMed ID: 10178392
    [No Abstract] [Full Text] [Related]

  • 16. Pharmaceuticals and medical devices: medical devices.
    Berry MD.
    Issue Brief Health Policy Track Serv; 2013 Dec 30; ():1-49. PubMed ID: 24482892
    [No Abstract] [Full Text] [Related]

  • 17. Defending substantial equivalence: an argument for the continuing validity of the 510(k) premarket notification process.
    Flaherty JM.
    Food Drug Law J; 2008 Dec 30; 63(4):901-27. PubMed ID: 19601388
    [No Abstract] [Full Text] [Related]

  • 18. Pharmaceuticals and Medical Devices: FDA Oversight.
    Berry MD, White RS, Thomson Reuters Accelus.
    Issue Brief Health Policy Track Serv; 2016 Dec 27; 2016():1-59. PubMed ID: 28252888
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Gastroenterology and urology devices; effective date of requirement for premarket approval of the implanted mechanical/hydraulic urinary continence device. Food and Drug Administration, HHS. Final rule.
    Fed Regist; 2000 Sep 26; 65(187):57726-32. PubMed ID: 11503643
    [Abstract] [Full Text] [Related]

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