184 related articles for article (PubMed ID: 10129629)
1. Medical devices; reclassification and codification of natural nonabsorbable silk surgical suture--FDA. Final rule.
Fed Regist; 1993 Oct; 58(205):57557-8. PubMed ID: 10129629
[TBL] [Abstract][Full Text] [Related]
2. Medical devices; reclassification and codification of the nonabsorbable expanded polytetrafluoroethylene surgical suture. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Apr; 65(75):20734-5. PubMed ID: 11010640
[TBL] [Abstract][Full Text] [Related]
3. Medical devices; reclassification and codification of absorbable poly(glycolide/L-lactide) surgical suture--FDA. Final rule.
Fed Regist; 1991 Sep; 56(181):47150-1. PubMed ID: 10114363
[TBL] [Abstract][Full Text] [Related]
4. Medical devices; reclassification and codification of the stainless steel suture. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Apr; 65(72):19835-6. PubMed ID: 11010635
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Medical devices; reclassification and codification of microsurgical argon laser for rhinology and laryngology--FDA. Final rule.
Fed Regist; 1993 May; 58(97):29533-4. PubMed ID: 10126115
[TBL] [Abstract][Full Text] [Related]
7. Medical devices: reclassification and codification of the absorbable polydioxanone surgical suture. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Dec; 67(244):77675-7. PubMed ID: 12492104
[TBL] [Abstract][Full Text] [Related]
8. Medical devices; reclassification and codification of hip joint metal polymer/metal semi-constrained porous-coated uncemented prosthesis--FDA. Final rule.
Fed Regist; 1993 Jan; 58(5):3227-8. PubMed ID: 10123372
[TBL] [Abstract][Full Text] [Related]
9. Medical devices; reclassification and codification of vitamin D test system--FDA. Final rule.
Fed Regist; 1998 Jul; 63(145):40364-6. PubMed ID: 10181714
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Obstetric and gynecologic devices; reclassification and classification of medical devices used for in vitro fertilization and related assisted reproduction procedures--FDA. Final rule.
Fed Regist; 1998 Sep; 63(175):48428-37. PubMed ID: 10182829
[TBL] [Abstract][Full Text] [Related]
12. Magnetic resonance diagnostic device; panel recommendation and report on petitions for magnetic resonance reclassification and codification of reclassification--FDA. Final rule.
Fed Regist; 1989 Feb; 54(20):5077-8. PubMed ID: 10291710
[TBL] [Abstract][Full Text] [Related]
13. Medical devices; designation of special control for eight surgical suture devices. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2003 Jun; 68(106):32983-5. PubMed ID: 12784826
[TBL] [Abstract][Full Text] [Related]
14. Medical devices; reclassification and codification of Neodymium:Yttrium:Aluminum:Garnet (Nd:YAG) Laser for peripheral iridotomy. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Feb; 65(29):6893-4. PubMed ID: 11010651
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Medical devices; reclassification of tumor-associated antigen immunological test system--FDA. Final rule.
Fed Regist; 1997 Dec; 62(242):66003-5. PubMed ID: 10179301
[TBL] [Abstract][Full Text] [Related]
17. Cardiovascular, orthopedic, and physical medicine diagnostic devices; reclassification of cardiopulmonary bypass accessory equipment, goniometer device, and electrode cable devices. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2000 Apr; 65(70):19317-9. PubMed ID: 11010630
[TBL] [Abstract][Full Text] [Related]
18. Medical devices; reclassification of polymethylmethacrylate (PMMA) bone cement. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Jul; 67(137):46852-5. PubMed ID: 12125716
[TBL] [Abstract][Full Text] [Related]
19. Medical devices; general and plastic surgery devices; classification of absorbable poly(hydroxybutyrate) surgical suture produced by recombinant DNA technology. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2007 Aug; 72(149):43144-6. PubMed ID: 17682290
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
