These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 1401559)

  • 1. The Safe Medical Device Act of 1990--ethical dilemmas for nurses.
    Miller I; Kjervik DK
    J Prof Nurs; 1992; 8(5):260. PubMed ID: 1401559
    [No Abstract]   [Full Text] [Related]  

  • 2. The Safe Medical Devices Act: what it means in practice.
    DiMotto J
    Nurs Qual Connect; 1993; 3(3):1, 5. PubMed ID: 8274957
    [No Abstract]   [Full Text] [Related]  

  • 3. Safe Medical Devices Act of 1990.
    Samuel FE
    Health Aff (Millwood); 1991; 10(1):192-5. PubMed ID: 2045049
    [No Abstract]   [Full Text] [Related]  

  • 4. User reporting under the Safe Medical Devices Act.
    Arcarese JS
    ANNA J; 1991 Oct; 18(5):466. PubMed ID: 1953082
    [No Abstract]   [Full Text] [Related]  

  • 5. The Safe Medical Devices Act of 1990--FDA. Notice.
    Fed Regist; 1991 Apr; 56(66):14111-3. PubMed ID: 10111151
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The safety of medical devices and the role of the FDA.
    Pillar B
    Nurs Econ; 1991; 9(4):284-6. PubMed ID: 1922433
    [No Abstract]   [Full Text] [Related]  

  • 7. Medical devices; preemption of state product liability claims--FDA. Withdrawal of proposed rule.
    Fed Regist; 1998 Jul; 63(142):39789-90. PubMed ID: 10181516
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preemption and medical devices: a response to Adler and Mann.
    Hermann M; Ritts GJ
    Food Drug Law J; 1996; 51(1):1-19. PubMed ID: 11794345
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Medical device reporting: the US final rule.
    Donawa ME
    Med Device Technol; 1996 Mar; 7(2):14-6, 18, 20-1. PubMed ID: 10159867
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Letters from Washington. Food and Drug Administration and medical technology: at an impasse?].
    Gelijns AC
    Ned Tijdschr Geneeskd; 1993 Jan; 137(3):146-50. PubMed ID: 8423866
    [No Abstract]   [Full Text] [Related]  

  • 11. Medical devices; preemption of state product liability claims--FDA. Correction.
    Fed Regist; 1997 Dec; 62(242):66179. PubMed ID: 10179302
    [No Abstract]   [Full Text] [Related]  

  • 12. The Safe Medical Devices Act.
    Clemens AM; Woo P
    Natl Med Leg J; 1993; 4(3):1, 7. PubMed ID: 8343564
    [No Abstract]   [Full Text] [Related]  

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

  • 14. Medical devices; preemption of state product liability claims--FDA. Proposed rule.
    Fed Regist; 1997 Dec; 62(239):65384-8. PubMed ID: 10176832
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Drug and device litigation in the 21st century.
    Svitak LS; Goss PJ
    Spec Law Dig Health Care Law; 2001 Nov; (271):9-36. PubMed ID: 11802352
    [No Abstract]   [Full Text] [Related]  

  • 16. Medical devices; procedures for premarket notification, premarket approval, classification, performance standards establishment, banning devices, and availability of regulatory hearings--FDA. Final rule.
    Fed Regist; 1992 Dec; 57(238):58400-6. PubMed ID: 10123143
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Postmarket surveillance for medical devices: America's new strategy.
    Normand SL; Hatfield L; Drozda J; Resnic FS
    BMJ; 2012 Oct; 345():e6848. PubMed ID: 23060660
    [No Abstract]   [Full Text] [Related]  

  • 18. Medical device reporting. A pilot study of nurses.
    George VD; Boruch RF
    AORN J; 1989 Mar; 49(3):815-9, 822-4, 826-7. PubMed ID: 2923435
    [No Abstract]   [Full Text] [Related]  

  • 19. Congress seeks to ensure safe medical devices.
    Collins M
    Trustee; 1990 Jan; 43(1):3. PubMed ID: 10103486
    [No Abstract]   [Full Text] [Related]  

  • 20. Primer on medical device regulation. Part II. Regulation of medical devices by the U.S. Food and Drug Administration.
    Monsein LH
    Radiology; 1997 Oct; 205(1):10-8. PubMed ID: 9314953
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.