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.
103 related articles for article (PubMed ID: 24358519)
1. FDA publishes battery survey results. Health Devices; 2013 Nov; 42(11):386. PubMed ID: 24358519 [No Abstract] [Full Text] [Related]
2. FDA publishes list of Y2K high-risk medical equipment. Hosp Case Manag; 1999 Aug; 7(8):144-6. PubMed ID: 10557731 [No Abstract] [Full Text] [Related]
3. FDA publishes checklist of Y2K high-risk devices. Healthc Benchmarks; 1999 Sep; 6(9):99-102. PubMed ID: 10557417 [TBL] [Abstract][Full Text] [Related]
4. Who would be affected if the FDA publishes mandatory standards? Or. . . Why Congress should get the FDA "off the hook". Miller MJ Med Instrum; 1986; 20(3):168. PubMed ID: 3724593 [No Abstract] [Full Text] [Related]
5. Cutting a battery pack cable can start a fire. Mirsaidi N Nursing; 2008 Aug; 38(8):13-4. PubMed ID: 18648273 [No Abstract] [Full Text] [Related]
6. Medical device batteries: ubiquitous and problematic. Lipschultz A Biomed Instrum Technol; 2013; 47(6):494-8. PubMed ID: 24328971 [No Abstract] [Full Text] [Related]
7. Defibrillators made by St Jude Medical are prone to battery failure, FDA warns. McCarthy M BMJ; 2016 Oct; 355():i5571. PubMed ID: 27742620 [No Abstract] [Full Text] [Related]
8. FDA provides important planning information. Stewart M Am Nurse; 1999; 31(5):23. PubMed ID: 10876409 [No Abstract] [Full Text] [Related]
9. An overview of MIS incidents reported to the FDA. Minim Invasive Surg Nurs; 1995; 9(2):59-73. PubMed ID: 7663582 [No Abstract] [Full Text] [Related]
10. 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]
11. FDA & Y2K. Preparing for the new millennium. Lewis C FDA Consum; 1999; 33(6):6-11. PubMed ID: 10628310 [No Abstract] [Full Text] [Related]
12. The FDA and the medical device approval process. Guez G; Garg A Dent Implantol Update; 2012 May; 23(5):33-7. PubMed ID: 22594003 [No Abstract] [Full Text] [Related]
13. 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]
14. FDA issues warning for battery-powered mobile medical carts. Health Manag Technol; 2017 Feb; 38(2):30. PubMed ID: 29474035 [No Abstract] [Full Text] [Related]
15. Ball is in providers' court. UDI system aims to help FDA identify problem products more quickly. Lee J Mod Healthc; 2012 Jul; 42(30):12, 14. PubMed ID: 22950261 [No Abstract] [Full Text] [Related]
16. FDA releases Y2K list of critical medical devices. Hosp Peer Rev; 1999 Sep; 24(9):138, 143. PubMed ID: 10558180 [No Abstract] [Full Text] [Related]
17. 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]
18. Bayesian statistics in medical devices: innovation sparked by the FDA. Campbell G J Biopharm Stat; 2011 Sep; 21(5):871-87. PubMed ID: 21830920 [TBL] [Abstract][Full Text] [Related]
19. Analysis of automated external defibrillator device failures reported to the Food and Drug Administration. DeLuca LA; Simpson A; Beskind D; Grall K; Stoneking L; Stolz U; Spaite DW; Panchal AR; Denninghoff KR Ann Emerg Med; 2012 Feb; 59(2):103-11. PubMed ID: 21872969 [TBL] [Abstract][Full Text] [Related]
20. Medical devices; device tracking. Final rule. Food and Drug Administration, HHS Fed Regist; 2002 Feb; 67(27):5943-52. PubMed ID: 11838471 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]