131 related articles for article (PubMed ID: 24839854)
21. [Discussion about Supervision Model of Customized Medical Device].
Sun J; Wu J; Qian H; Liu B; Zhang S
Zhongguo Yi Liao Qi Xie Za Zhi; 2017 Nov; 41(6):432-435. PubMed ID: 29862704
[TBL] [Abstract][Full Text] [Related]
22. A pivotal medical-device case.
Picca SM
N Engl J Med; 2008 Apr; 358(16):1758. PubMed ID: 18426011
[No Abstract] [Full Text] [Related]
23. A pivotal medical-device case.
Greenspan H
N Engl J Med; 2008 Apr; 358(16):1758. PubMed ID: 18420514
[No Abstract] [Full Text] [Related]
24. Medical devices; establishment registration and device listing for manufacturers and distributors of devices--FDA. Direct final rule.
Fed Regist; 1998 Sep; 63(188):51825-7. PubMed ID: 10185812
[TBL] [Abstract][Full Text] [Related]
25. [Clinical trial requests of indigenous diagnostic imaging ultrasound devices in first-time registration application].
Guo Z; Cao G; Tao K
Zhongguo Yi Liao Qi Xie Za Zhi; 2012 Nov; 36(6):438-40. PubMed ID: 23461122
[TBL] [Abstract][Full Text] [Related]
26. Medical devices; pediatric uses of devices; requirement for submission of information on pediatric subpopulations that suffer from a disease or condition that a device is intended to treat, diagnose, or cure. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2014 Jan; 79(7):1735-41. PubMed ID: 24409553
[TBL] [Abstract][Full Text] [Related]
27. Medical devices; medical device reporting; baseline reports. Direct final rule.
Food and Drug Administration, HHS
Fed Regist; 2008 Jun; 73(115):33692-5. PubMed ID: 18677824
[TBL] [Abstract][Full Text] [Related]
28. Medical devices; exemption from premarket notification requirements; class I devices; technical amendment. Final rule; technical amendment.
Food and Drug Administration. HHS
Fed Regist; 2001 Jul; 66(143):38786-819. PubMed ID: 11725800
[TBL] [Abstract][Full Text] [Related]
29. An assessment of the regulations on medical devices in the European Union.
Frank S
Food Drug Law J; 2001; 56(1):99-122. PubMed ID: 11942353
[No Abstract] [Full Text] [Related]
30. When to conduct a clinical trial.
Boutrand JP
Med Device Technol; 2004 Oct; 15(8):28-31. PubMed ID: 16225271
[TBL] [Abstract][Full Text] [Related]
31. [Approval Status and Suggestions on Supervision of Class II Innovative Medical Device].
Duan S; Zhong Z
Zhongguo Yi Liao Qi Xie Za Zhi; 2023 Jan; 47(1):80-82. PubMed ID: 36752012
[TBL] [Abstract][Full Text] [Related]
32. [Medical device registration system comparison between China and U.S.A].
Yue W
Zhongguo Yi Liao Qi Xie Za Zhi; 2009 Jan; 33(1):51-8. PubMed ID: 19459353
[TBL] [Abstract][Full Text] [Related]
33. [Medical innovations in the area of conflict between certification and allowance].
Möller B; Stockheim M; Kraus T; Weber A
Dtsch Med Wochenschr; 2010 Oct; 135(42):2088-92. PubMed ID: 20941684
[TBL] [Abstract][Full Text] [Related]
34. The Canadian perspective: trends in drug and medical device class actions in Canada.
Vernon W
Food Drug Law J; 2006; 61(3):569-76. PubMed ID: 16989040
[No Abstract] [Full Text] [Related]
35. Medical devices; establishment registration and device listing for manufacturers and distributors of devices; companion to direct final rule--FDA. Proposed rule.
Fed Regist; 1998 Sep; 63(188):51874-5. PubMed ID: 10185813
[TBL] [Abstract][Full Text] [Related]
36. Approval of an alternative requirement of the Mammography Quality Standards Act; availability--FDA. Notice.
Fed Regist; 1998 Nov; 63(216 Pt 1):60352. PubMed ID: 10187394
[TBL] [Abstract][Full Text] [Related]
37. A pivotal medical-device case.
Curfman GD; Morrissey S; Drazen JM
N Engl J Med; 2008 Jan; 358(1):76-7. PubMed ID: 18172178
[No Abstract] [Full Text] [Related]
38. Medical devices: reports of corrections and removals; delay of effective data--FDA. Direct final rule; delay of effective date.
Fed Regist; 1998 Nov; 63(222):63983. PubMed ID: 10339047
[TBL] [Abstract][Full Text] [Related]
39. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Final rule.
Fed Regist; 1998 Oct; 63(195):54042-4. PubMed ID: 10185825
[TBL] [Abstract][Full Text] [Related]
40. Medical device regulations and testing for toxicologic pathologists.
Schuh JC
Toxicol Pathol; 2008 Jan; 36(1):63-9. PubMed ID: 18337222
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
