362 related articles for article (PubMed ID: 11010635)
1. 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]
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 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Medical devices; ear, nose and throat devices; reclassification of the endolymphatic shunt tube with valve. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Apr; 67(82):20893-4. PubMed ID: 11980454
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Medical devices; reclassification of the shoulder joint metal/polymer/metal nonconstrained or semi-constrained porous-coated uncemented prosthesis. Food and Drug Administration, HHS. Final rule.
Fed Regist; 2001 Feb; 66(40):12734-7. PubMed ID: 11503865
[TBL] [Abstract][Full Text] [Related]
16. Cardiovascular devices; reclassification of certain percutaneous transluminal coronary angioplasty (PTCA) catheters. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2010 Sep; 75(173):54493-6. PubMed ID: 20824947
[TBL] [Abstract][Full Text] [Related]
17. Microbiology devices; reclassification of herpes simplex virus types 1 and 2 serological assays. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2007 Apr; 72(63):15828-30. PubMed ID: 17455387
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Medical devices; reclassification of three anesthesiology preamendments class III devices into class II. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2001 Nov; 66(221):57366-8. PubMed ID: 11776278
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
