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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

320 related items for PubMed ID: 15532863

  • 1. Facilities' responsibilities after notification of a medical device hazard or recall.
    Health Devices; 2004 Sep; 33(9):339. PubMed ID: 15532863
    [No Abstract] [Full Text] [Related]

  • 2. The FDA moves to implement the Safe Medical Devices Act.
    Tamborlane T.
    Healthspan; 1992 Nov; 9(10):7-10. PubMed ID: 10122957
    [No Abstract] [Full Text] [Related]

  • 3. Medical device epidemiology and surveillance: patient safety is the bottom line.
    Brown SL, Bright RA, Tavris DR.
    Expert Rev Med Devices; 2004 Sep; 1(1):1-2. PubMed ID: 16293003
    [No Abstract] [Full Text] [Related]

  • 4. Challenges in regulating breakthrough medical devices.
    Muni NI, Gross TP, Boam AB, Wang S, Zuckerman BD.
    Food Drug Law J; 2005 Sep; 60(2):137-42. PubMed ID: 16097092
    [No Abstract] [Full Text] [Related]

  • 5. Medical device reports raise and red flag.
    Miles F, Miles JF.
    Provider; 1997 Jan; 23(1):53, 55-6. PubMed ID: 10166155
    [No Abstract] [Full Text] [Related]

  • 6. Two-page FDA form eases device-act compliance.
    Benson JS.
    Health Facil Manage; 1992 Feb; 5(2):40-7. PubMed ID: 10116138
    [No Abstract] [Full Text] [Related]

  • 7. AHA comments to FDA on Safe Devices Act.
    DePorter J.
    Mater Manag Health Care; 1992 Apr; 1(2):18-21. PubMed ID: 10125489
    [No Abstract] [Full Text] [Related]

  • 8. Facilities strive to comply with new Act. The long-term effects of the Safe Medical Devices Act are still unknown.
    Schuster DK, Butler KH.
    Health Prog; 1993 May; 74(4):53-7. PubMed ID: 10125364
    [Abstract] [Full Text] [Related]

  • 9. Medical device recalls from 2004 to 2006: a focus on Class I recalls.
    Villarraga ML, Guerin HL, Lam T.
    Food Drug Law J; 2007 May; 62(3):581-92. PubMed ID: 17915400
    [No Abstract] [Full Text] [Related]

  • 10. New FDA reporting rule means new concerns.
    Healthc Hazard Mater Manage; 1996 Mar; 9(6):1-4. PubMed ID: 10155771
    [No Abstract] [Full Text] [Related]

  • 11. Medical device safety: FDA's postmarket transformation initiative.
    Schultz D.
    Food Drug Law J; 2007 Mar; 62(3):593-6. PubMed ID: 17915401
    [No Abstract] [Full Text] [Related]

  • 12. Update on the Safe Medical Devices Act of 1990: current hospital requirements and recommended actions 1996.
    Berek B.
    Healthc Facil Manag Ser; 1996 Jul; ():1-18. PubMed ID: 10159144
    [Abstract] [Full Text] [Related]

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  • 14. Questions and answers about tracking program.
    OR Manager; 1994 Apr; 10(4):13-4. PubMed ID: 10133243
    [No Abstract] [Full Text] [Related]

  • 15. New medical devices reporting requirements.
    Carley MM.
    Contemp Longterm Care; 1991 Dec; 14(12):66, 68. PubMed ID: 10117951
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Global harmonization--a catalyst for safety.
    Jacques T.
    Occup Health Saf; 2010 May; 79(5):48-9. PubMed ID: 20491303
    [No Abstract] [Full Text] [Related]

  • 18. European requirements for product returns.
    Donawa M.
    Med Device Technol; 2005 Nov; 16(9):28-31. PubMed ID: 16438446
    [Abstract] [Full Text] [Related]

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    ; . PubMed ID:
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  • 20. Users to report device-related deaths to FDA.
    OR Manager; 1991 Jan; 7(1):1, 13. PubMed ID: 10110321
    [No Abstract] [Full Text] [Related]

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