961 related articles for article (PubMed ID: 11010655)
1. 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]
2. 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]
3. 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]
4. 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]
5. Medical devices; exemptions from premarket notification; class II devices; vascular tunnelers. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Mar; 65(43):11466-7. PubMed ID: 11010650
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Dental devices; dental noble metal alloys and dental base metal alloys; designation of special controls. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2004 Aug; 69(162):51765-6. PubMed ID: 15329980
[TBL] [Abstract][Full Text] [Related]
10. Ear, nose, and throat devices; classification of the nasal dilator, the intranasal splint, and the bone particle collector. Food and Drug Administration, HHS. Final rule.
Fed Regist; 1999 Mar; 64(44):10947-9. PubMed ID: 10557619
[TBL] [Abstract][Full Text] [Related]
11. Medical devices; exemption from premarket notification; class II devices; triiodothyronine test system. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Oct; 65(202):62285-6. PubMed ID: 11503681
[TBL] [Abstract][Full Text] [Related]
12. Medical Device; exemption from premarket notification; class II devices; pharmacy compounding systems. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2001 Mar; 66(55):15796-8. PubMed ID: 11706859
[TBL] [Abstract][Full Text] [Related]
13. Medical device; exemption from premarket notification; class II devices; barium enema retention catheters and tips with or without a bag. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Dec; 65(237):76930-2. PubMed ID: 11503724
[TBL] [Abstract][Full Text] [Related]
14. Medical devices; implementation of third party review under the Food and Drug Administration Modernization Act of 1997; emergency processing request under OMB review--FDA. Notice.
Fed Regist; 1998 May; 63(99):28388-91. PubMed ID: 10179874
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Medical devices; reclassification and codification of suction lipoplasty system for aesthetic body contouring--FDA. Final rule.
Fed Regist; 1998 Feb; 63(31):7703-5. PubMed ID: 10177951
[TBL] [Abstract][Full Text] [Related]
17. Medical devices; device tracking--FDA. Final rule; suspension of effective date; notification of status under the Safe Medical Devices Act; technical amendments.
Fed Regist; 1993 Aug; 58(156):43442-51. PubMed ID: 10127886
[TBL] [Abstract][Full Text] [Related]
18. Medical devices; reprocessed single-use devices; requirement for submission of validation data. Direct final rule.
Food and Drug Administration, HHS
Fed Regist; 2006 Sep; 71(185):55729-37. PubMed ID: 17017469
[TBL] [Abstract][Full Text] [Related]
19. Medical devices; procedures for premarket notification, premarket approval, classification, performance standards establishment, banning devices, and availability of regulatory hearings--FDA. Final rule.
Fed Regist; 1992 Dec; 57(238):58400-6. PubMed ID: 10123143
[TBL] [Abstract][Full Text] [Related]
20. Medical devices; 30-day notices and 135-day PMA (premarket approval application) supplement review--FDA. Direct final rule.
Fed Regist; 1998 Apr; 63(80 Pt 1):20530-3. PubMed ID: 10179319
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]