167 related articles for article (PubMed ID: 16528829)
1. Medical device and radiological health regulations come of age.
Rados C
FDA Consum; 2006; 40(1):58-65. PubMed ID: 16528829
[No Abstract] [Full Text] [Related]
2. Food and Drug Administration control of medical devices: an inescapable intrusion and stimulus for adaptation.
Friedman EA
ASAIO J; 1998; 44(4):239-40. PubMed ID: 9682946
[No Abstract] [Full Text] [Related]
3. Old customs, ancient lore: the development of custom device law through neglect.
Klepinski RJ
Food Drug Law J; 2006; 61(2):237-49. PubMed ID: 16903030
[No Abstract] [Full Text] [Related]
4. Defending substantial equivalence: an argument for the continuing validity of the 510(k) premarket notification process.
Flaherty JM
Food Drug Law J; 2008; 63(4):901-27. PubMed ID: 19601388
[No Abstract] [Full Text] [Related]
5. 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]
6. Shrinking waters in the safe harbor: has Integra Lifesciences v. Merck turned the tide by narrowing available exempted infringing uses?
Davison AM
Food Drug Law J; 2004; 59(1):79-92. PubMed ID: 15190926
[No Abstract] [Full Text] [Related]
7. Encouraging medical device innovation: reimbursement problems and new policies.
Robinson CA; Hoyer TE; Ault TA
Public Health Rep; 1996; 111(5):468-70. PubMed ID: 8837637
[No Abstract] [Full Text] [Related]
8. [Standards used in the regulation of medical device in USA].
Hu W; Gu H
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2007 Nov; 21(11):1263-7. PubMed ID: 18069490
[TBL] [Abstract][Full Text] [Related]
9. Medical device reporting: issues with Class III medical devices.
Zigler J; Walsh J; Zigler J
Food Drug Law J; 2007; 62(3):573-80. PubMed ID: 17915398
[No Abstract] [Full Text] [Related]
10. Access to clinical devices through nontraditional routes.
Klepinski RJ
Food Drug Law J; 2007; 62(4):849-63. PubMed ID: 18557233
[No Abstract] [Full Text] [Related]
11. Supplemental applications proposing labeling changes for approved drugs, biologics, and medical devices. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2008 Aug; 73(164):49603-10. PubMed ID: 18958946
[TBL] [Abstract][Full Text] [Related]
12. History of breast implants and the food and drug administration.
Spear SL; Parikh PM; Goldstein JA
Clin Plast Surg; 2009 Jan; 36(1):15-21, v. PubMed ID: 19055957
[TBL] [Abstract][Full Text] [Related]
13. Combination products regulation at the FDA.
Lauritsen KJ; Nguyen T
Clin Pharmacol Ther; 2009 May; 85(5):468-70. PubMed ID: 19381151
[TBL] [Abstract][Full Text] [Related]
14. Hospitals gain ground in Medicare device flap.
Scott L
Mod Healthc; 1996 Apr; 26(17):2, 12. PubMed ID: 10157128
[No Abstract] [Full Text] [Related]
15. Pharmaceuticals and medical devices: medical devices. Year end issue brief.
Tiffany S
Issue Brief Health Policy Track Serv; 2008 Jan; ():1-19. PubMed ID: 18345548
[No Abstract] [Full Text] [Related]
16. Commemorating the 40th Anniversary of the 1976 Medical Device Amendments.
Junod S
Food Drug Law J; 2017; 72(1):26-31. PubMed ID: 29140652
[No Abstract] [Full Text] [Related]
17. Pharmaceuticals and medical devices: medical devices.
Chaps NA
Issue Brief Health Policy Track Serv; 2009 Jan; ():1-23. PubMed ID: 19297720
[No Abstract] [Full Text] [Related]
18. The US medical device bundling policy.
Donawa M
Med Device Technol; 2004 Nov; 15(9):25-7. PubMed ID: 16231784
[TBL] [Abstract][Full Text] [Related]
19. Strategic planning for U.S. premarket approval submissions.
Donawa M
Med Device Technol; 2006 Sep; 17(7):21-3. PubMed ID: 17039953
[TBL] [Abstract][Full Text] [Related]
20. FDA Device Regulation.
Lauer M; Barker JP; Solano M; Dubin J
Mo Med; 2017; 114(4):283-288. PubMed ID: 30228612
[No Abstract] [Full Text] [Related]
[Next] [New Search]