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 *

314 related articles for article (PubMed ID: 10312180)

  • 1. A "complaint department" for medical devices.
    Thompson RC
    FDA Consum; 1987 Mar; 21(2):10-3. PubMed ID: 10312180
    [No Abstract]   [Full Text] [Related]  

  • 2. Looking for trouble in medical devices.
    Stearman DW
    FDA Consum; 1987 Sep; 21(7):18-23. PubMed ID: 10312181
    [No Abstract]   [Full Text] [Related]  

  • 3. The Safe Medical Devices Act: gauging impact on hospitals.
    DePorter J
    Trustee; 1992 Dec; 45(12):19-20. PubMed ID: 10122636
    [No Abstract]   [Full Text] [Related]  

  • 4. Hospitals wary of interpretation of medical device reporting law.
    Burke M
    Hospitals; 1991 Oct; 65(20):40, 42. PubMed ID: 1916713
    [No Abstract]   [Full Text] [Related]  

  • 5. Experts see dangers in rules implementing Safe Medical Devices Act.
    Wagner M
    Mod Healthc; 1992 Feb; 22(7):36-9. PubMed ID: 10116238
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Safe Medical Devices Act of 1990: current hospital requirements and recommended actions.
    Alder H
    Healthc Facil Manag Ser; 1993 Sep; ():1-34. PubMed ID: 10132639
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MedWatch. On lookout for medical product problems.
    Ropp KL
    FDA Consum; 1993 Nov; 27(9):14-7. PubMed ID: 10130376
    [No Abstract]   [Full Text] [Related]  

  • 8. Food and Drug Administration--General hospital and personal use devices; general provisions. Final rule.
    Fed Regist; 1980 Oct; 45(205):69678-737. PubMed ID: 10248451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Manufacturer-hospital collaboration to improve patient care quality.
    DeGasparis P; Magill KA; Milone T
    Hosp Top; 1983; 61(4):15-6. PubMed ID: 10260122
    [No Abstract]   [Full Text] [Related]  

  • 10. Feds focus on medical devices.
    Goldfarb B; Wolfberg D
    JEMS; 1992 Jul; 17(7):35-8, 45-7. PubMed ID: 10120068
    [No Abstract]   [Full Text] [Related]  

  • 11. Report device failures to the FDA.
    JCAH Perspect; 1987; 7(7-8):5-7. PubMed ID: 10289785
    [No Abstract]   [Full Text] [Related]  

  • 12. Not enough warning. GAO report finds FDA's medical device monitoring lacking.
    Hensley S
    Mod Healthc; 1997 Mar; 27(10):102, 104. PubMed ID: 10165267
    [No Abstract]   [Full Text] [Related]  

  • 13. Reporting dangerous and unsafe medical devices.
    Wall MT
    Healthtexas; 1991 May; 46(11):14. PubMed ID: 10111562
    [No Abstract]   [Full Text] [Related]  

  • 14. Patient calls not annunciated when Rauland Responder IV nurse call system is in All Page mode.
    Health Devices; 2001 Aug; 30(8):314-5. PubMed ID: 11544780
    [No Abstract]   [Full Text] [Related]  

  • 15. Generating change. Health Devices motivates suppliers to improve their products.
    Health Devices; 2001 Jun; 30(6):197-9. PubMed ID: 11447864
    [No Abstract]   [Full Text] [Related]  

  • 16. Reuse of single-use medical devices.
    Fielder JH
    IEEE Eng Med Biol Mag; 1999; 18(6):80-1. PubMed ID: 10576078
    [No Abstract]   [Full Text] [Related]  

  • 17. FDA works to reduce preventable medical device injuries.
    Rados C
    FDA Consum; 2003; 37(4):29-33. PubMed ID: 12971346
    [No Abstract]   [Full Text] [Related]  

  • 18. Cribs.
    Nobel JJ
    Pediatr Emerg Care; 1992 Apr; 8(2):110-2. PubMed ID: 1603701
    [No Abstract]   [Full Text] [Related]  

  • 19. Myths and realities in medical packaging.
    Pilchik R
    Med Device Technol; 2003 Mar; 14(2):16-7. PubMed ID: 12698692
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MEDWATCH: the new FDA medical products reporting program.
    Kennedy DL
    Respir Care; 1993 Oct; 38(10):1077-80. PubMed ID: 10145891
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 16.