453 related articles for article (PubMed ID: 10291347)
1. Medical devices; intent to initiate proceedings to establish effective dates of requirement for premarket approval for 31 class III preamendments devices--FDA. Advance notice of proposed rulemaking.
Fed Regist; 1989 Jan; 54(4):550-2. PubMed ID: 10291347
[TBL] [Abstract][Full Text] [Related]
2. Medical devices; retention in class III and effective date of requirement for premarket approval for three preamendments class III devices--FDA. Proposed rule; opportunity to request a change in classification.
Fed Regist; 1998 Jul; 63(146):40673-7. PubMed ID: 10181520
[TBL] [Abstract][Full Text] [Related]
3. Medical devices; exemption from premarket notification and reserved devices; class I. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Jan; 65(10):2296-323. PubMed ID: 11010655
[TBL] [Abstract][Full Text] [Related]
4. Medical devices; effective date of requirement for premarket approval for three class III preamendments physical medicine devices--FDA. Proposed rule; opportunity to request a change in classification.
Fed Regist; 1998 Jul; 63(146):40677-81. PubMed ID: 10181521
[TBL] [Abstract][Full Text] [Related]
5. Medical devices; exemptions from premarket notification and reserved devices; class I--FDA. Notice.
Fed Regist; 1998 Feb; 63(21):5387-93. PubMed ID: 10177333
[TBL] [Abstract][Full Text] [Related]
6. Medical devices; exemption from premarket notification and reserved devices; Class I--FDA. Proposed rule.
Fed Regist; 1998 Nov; 63(218):63222-53. PubMed ID: 10187398
[TBL] [Abstract][Full Text] [Related]
7. Medical devices; effective date of requirement for premarket approval for three class III preamendments devices--FDA. Proposed rule; opportunity to request a change in classification.
Fed Regist; 1998 Aug; 63(159):44177-81. PubMed ID: 10184983
[TBL] [Abstract][Full Text] [Related]
8. Medical devices; effective date of requirement for premarket approval for three class III preamendments devices. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2004 Jun; 69(120):34917-20. PubMed ID: 15224687
[TBL] [Abstract][Full Text] [Related]
9. Gastroenterology-urology devices; effective date of requirement for premarket approval of the penile inflatable implant. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Apr; 65(71):19650-8. PubMed ID: 11010632
[TBL] [Abstract][Full Text] [Related]
10. Medical devices; effective date of requirement for premarket approval for a class III preamendments obstetrical and gynecological device. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Jul; 65(129):41330-2. PubMed ID: 11067678
[TBL] [Abstract][Full Text] [Related]
11. Effective date of requirement for premarket approval for three class III preamendments devices. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2011 Aug; 76(158):50663-7. PubMed ID: 21845785
[TBL] [Abstract][Full Text] [Related]
12. Medical devices; exemptions from premarket notification; class II devices--FDA, Final rule.
Fed Regist; 1998 Nov; 63(212):59222-31. PubMed ID: 10187384
[TBL] [Abstract][Full Text] [Related]
13. Policy statement; class II medical devices--FDA. Notice.
Fed Regist; 1985 Oct; 50(205):43060-81. PubMed ID: 10274028
[TBL] [Abstract][Full Text] [Related]
14. General and plastic surgery devices; effective date of requirement for premarket approval of the silicone inflatable breast prosthesis. Department of Health and Human Services (HHS), Public Health Service (PHS), Food and Drug Administration (FDA). Final rule.
Fed Regist; 1999 Aug; 64(160):45155-61. PubMed ID: 10558602
[TBL] [Abstract][Full Text] [Related]
15. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices), guidance for FDA reviewers and industry; availability--FDA. Notice.
Fed Regist; 1998 Nov; 63(215):60009-10. PubMed ID: 10187389
[TBL] [Abstract][Full Text] [Related]
16. Dental devices; effective date of requirement for premarket approval; temporomandibular joint prostheses--FDA. Final rule.
Fed Regist; 1998 Dec; 63(250):71743-6. PubMed ID: 10339055
[TBL] [Abstract][Full Text] [Related]
17. Orthopedic devices: classification and reclassification of pedicle screw spinal systems--FDA. Final rule.
Fed Regist; 1998 Jul; 63(143):40025-41. PubMed ID: 10181517
[TBL] [Abstract][Full Text] [Related]
18. Gastroenterology and urology devices; effective date of requirement for premarket approval of the implanted mechanical/hydraulic urinary continence device. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Sep; 65(187):57726-32. PubMed ID: 11503643
[TBL] [Abstract][Full Text] [Related]
19. Health device legislation: an overview of the law and its impact on respiratory care.
Bancroft ML; Steen JA
Respir Care; 1978 Dec; 23(12):1179-84. PubMed ID: 10315033
[TBL] [Abstract][Full Text] [Related]
20. Guidance for the emergency use of unapproved medical devices; availability--FDA. Notice.
Fed Regist; 1985 Oct; 50(204):42866-7. PubMed ID: 10274027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
