Vas-Cath, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vas-Cath, Inc. Gastroenterology & Urology ✕
11 devices
Cleared
Aug 19, 1997
NIAGARA DUAL LUMEN CATHETER
Gastroenterology & Urology
238d
Cleared
Jul 01, 1993
VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS
Gastroenterology & Urology
653d
Cleared
Jul 01, 1993
VAS-CATH DUALATOR(TM) VESSEL DILATOR
Gastroenterology & Urology
651d
Cleared
Apr 09, 1991
VAS-CATH URETERAL STENTS CATHETER, MODIFICATION
Gastroenterology & Urology
137d
Cleared
Feb 09, 1990
FLEXXICON PLUS DUAL LUMEN DIALYSIS CATHETER
Gastroenterology & Urology
150d
Cleared
Oct 03, 1989
VAS-CATH URETERAL STENT CATHETER
Gastroenterology & Urology
81d
Cleared
Apr 11, 1989
MODIFIED VAS-CATH CATHETER REPAIR KIT
Gastroenterology & Urology
91d
Cleared
Apr 05, 1989
MODIFICATION HEMOFILTRATION CATHETER HF-100
Gastroenterology & Urology
51d
Cleared
Nov 14, 1988
VAS-CATH CATHETER REPAIR KIT
Gastroenterology & Urology
69d
Cleared
Jul 13, 1988
VAS-CATH PEDIATRIC HEMOFILTRATION CATHETER
Gastroenterology & Urology
28d
Cleared
Jun 23, 1988
VAS-CATH FLEXXICON DUAL LUMEN DIALYSIS CATHETER
Gastroenterology & Urology
62d