340 related articles for article (PubMed ID: 10187388)
1. General hospital and personal use devices: proposed classification of liquid chemical sterilants and general purpose disinfectants--FDA. Proposed rule.
Fed Regist; 1998 Nov; 63(215):59917-21. PubMed ID: 10187388
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Medical devices; general hospital and personal use devices; classification of the filtering facepiece respirator for use by the general public in public health medical emergencies. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2007 Jul; 72(127):36360-3. PubMed ID: 17674487
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Medical devices; classification/reclassification of immunohistochemistry reagents and kits--FDA. Final rule.
Fed Regist; 1998 Jun; 63(106):30132-42. PubMed ID: 10179865
[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. 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]
8. 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]
9. 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]
10. Medical devices; obstetrical and gynecological devices; classification of the breast lesion documentation system. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2003 Jul; 68(144):44413-5. PubMed ID: 12884877
[TBL] [Abstract][Full Text] [Related]
11. Neurological devices; classification of human dura mater. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2003 Dec; 68(243):70435-6. PubMed ID: 14682309
[TBL] [Abstract][Full Text] [Related]
12. Dental devices; classification for intraoral devices for snoring and/or obstructive sleep apnea. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Nov; 67(218):68510-2. PubMed ID: 12428642
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Medical devices; ear, nose, and throat devices; classification of the transcutaneous air conduction hearing aid system. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Nov; 67(216):67789-90. PubMed ID: 12422884
[TBL] [Abstract][Full Text] [Related]
16. Medical devices; neurological devices; classification of cranial orthosis--FDA. Final rule.
Fed Regist; 1998 Jul; 63(146):40650-2. PubMed ID: 10181519
[TBL] [Abstract][Full Text] [Related]
17. Medical devices; general and plastic surgery devices; classification of the low energy ultrasound wound cleaner. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2005 Nov; 70(214):67353-5. PubMed ID: 16273747
[TBL] [Abstract][Full Text] [Related]
18. Medical devices; classification/reclassification; restricted devices; analyte specific reagents--FDA. Final rule.
Fed Regist; 1997 Nov; 62(225):62243-60. PubMed ID: 10177056
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
