313 related articles for article (PubMed ID: 10285636)
1. Radiology devices; general provisions and classifications of 59 devices--FDA. Final rule.
Fed Regist; 1988 Jan; 53(12):1554-71. PubMed ID: 10285636
[TBL] [Abstract][Full Text] [Related]
2. Food and Drug Administration--General hospital and personal use devices; general provisions. Final rule.
Fed Regist; 1980 Oct; 45(205):69678-737. PubMed ID: 10248451
[TBL] [Abstract][Full Text] [Related]
3. Medical devices; classification for medical washer and medical washer-disinfector. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Nov; 67(221):69119-21. PubMed ID: 12437015
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Medical devices; medical device distributor reporting; opportunity for comments--FDA. Final rule; opportunity for comments.
Fed Regist; 1993 Sep; 58(168):46514. PubMed ID: 10128334
[TBL] [Abstract][Full Text] [Related]
6. Medical devices; gastroenterology-urology devices; nonimplanted, peripheral electrical continence device. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Apr; 65(68):18236-7. PubMed ID: 11010624
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Medical devices; medical device distributor reporting--FDA. Final rule; notification of status under the Safe Medical Devices Act; confirmation of effective date.
Fed Regist; 1993 Sep; 58(168):46514-23. PubMed ID: 10128335
[TBL] [Abstract][Full Text] [Related]
11. Medical devices; gastroenterology and urology devices; classification of the electrogastrography system. Food and Drug Administration, HHS. Final rule.
Fed Regist; 1999 Sep; 64(184):51442-4. PubMed ID: 11010709
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Medical devices; humanitarian use of devices--FDA. Final rule.
Fed Regist; 1998 Nov; 63(212):59217-22. PubMed ID: 10187383
[TBL] [Abstract][Full Text] [Related]
16. General hospital and personal use devices; classification of the Apgar timer, lice removal kit, and infusion stand--FDA. Proposed rule.
Fed Regist; 1998 Mar; 63(46):11632-3. PubMed ID: 10177746
[TBL] [Abstract][Full Text] [Related]
17. Medical devices; medical device, user facility, distributor, and manufacturer reporting, certification, and registration--FDA. Tentative final rule.
Fed Regist; 1991 Nov; 56(228):60024-39. PubMed ID: 10115705
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Medical devices; 30-day notices and 135-day PMA supplement review--FDA. Direct final rule; withdrawal.
Fed Regist; 1998 Aug; 63(154):42699. PubMed ID: 10182563
[TBL] [Abstract][Full Text] [Related]
20. Medical devices; illustrative and designated lists for device tracking--FDA. Final rule and request for comments.
Fed Regist; 1993 Aug; 58(156):43451-5. PubMed ID: 10171508
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]