239 related articles for article (PubMed ID: 9259343)
21. Medical Devices; hematology and pathology devices; reclassification of automated blood cell separator device operating by filtration principle from class III to class II. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2003 Feb; 68(40):9530-2. PubMed ID: 12617085
[TBL] [Abstract][Full Text] [Related]
22. Clinical validation of the non-invasive cardiac output monitor USCOM-1A in critically ill patients.
van Lelyveld-Haas LE; van Zanten AR; Borm GF; Tjan DH
Eur J Anaesthesiol; 2008 Nov; 25(11):917-24. PubMed ID: 18652712
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Comparison of FloTrac cardiac output monitoring system in patients undergoing coronary artery bypass grafting with pulmonary artery cardiac output measurements.
Cannesson M; Attof Y; Rosamel P; Joseph P; Bastien O; Lehot JJ
Eur J Anaesthesiol; 2007 Oct; 24(10):832-9. PubMed ID: 17666154
[TBL] [Abstract][Full Text] [Related]
25. [Pulmonary artery catheter--its utility and limitations].
Ohnishi Y
Masui; 2009 Jul; 58(7):884-90. PubMed ID: 19618830
[TBL] [Abstract][Full Text] [Related]
26. [Measurement of cardiac output after cardiac surgery: validation of a partial carbon dioxide rebreathing (NICO) system in comparison with continuous thermodilution with a pulmonary artery catheter].
Jover JL; Soro M; Belda FJ; Aguilar G; Caro P; Ferrandis R
Rev Esp Anestesiol Reanim; 2005 May; 52(5):256-62. PubMed ID: 15968903
[TBL] [Abstract][Full Text] [Related]
27. [Swan-Ganz catheter (pulmonary artery catheter)].
Neya K
Kyobu Geka; 2009 Jul; 62(8 Suppl):677-81. PubMed ID: 20715691
[TBL] [Abstract][Full Text] [Related]
28. Pulmonary artery thermodilution cardiac output vs. transpulmonary thermodilution cardiac output in two patients with intrathoracic pathology.
Breukers RB; Jansen JR
Acta Anaesthesiol Scand; 2004 May; 48(5):658-61. PubMed ID: 15101866
[TBL] [Abstract][Full Text] [Related]
29. The nightmare of FDA clearance/approval to market: perception or reality?
Tylenda CA
Technol Health Care; 1996 Sep; 4(3):259-67. PubMed ID: 8931236
[TBL] [Abstract][Full Text] [Related]
30. Medical devices; apnea monitor; special controls. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Jul; 67(137):46851-2. PubMed ID: 12125715
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Medical devices; immunology and microbiology devices; classification of the endotoxin assay. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2003 Oct; 68(211):62007-8. PubMed ID: 14594019
[TBL] [Abstract][Full Text] [Related]
34. Medical devices; reclassification of the cutaneous carbon dioxide and the cutaneous oxygen monitor. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2002 Dec; 67(240):76678-81. PubMed ID: 12481766
[TBL] [Abstract][Full Text] [Related]
35. [Diagnostic kits in parasitology: which controls?].
Rossi P
Parassitologia; 2004 Jun; 46(1-2):145-9. PubMed ID: 15305705
[TBL] [Abstract][Full Text] [Related]
36. Medical devices; immunology and microbiology devices; classification of the immunomagnetic circulating cancer cell selection and enumeration system. Final rule.
Food and Drug Administration, HHS
Fed Regist; 2004 May; 69(91):26036-8. PubMed ID: 15137395
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Health device legislation: an overview of the law and its impact on respiratory care.
Bancroft ML; Steen JA
Respir Care; 1978 Dec; 23(12):1179-84. PubMed ID: 10315033
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]