Vas-Cath of Canada , Ltd. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Vas-Cath of Canada , Ltd. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1979 to 1988. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vas-Cath of Canada , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vas-Cath of Canada , Ltd.
19 devices
Cleared
Mar 02, 1988
LUER LOCK CONNECTORS / RIDIG P.V.C.
Gastroenterology & Urology
76d
Cleared
Jul 16, 1987
VAS-CATH PERITONEAL DIALYSIS CATHETER
Gastroenterology & Urology
66d
Cleared
Jun 12, 1987
VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH
Gastroenterology & Urology
58d
Cleared
Jun 12, 1987
VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH
Gastroenterology & Urology
58d
Cleared
Oct 24, 1986
VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY
General & Plastic Surgery
10d
Cleared
Aug 22, 1985
VACCESS TM 4006
Gastroenterology & Urology
17d
Cleared
May 21, 1985
OPTI-FLOW DIGITAL SUBTRACTION ANGIOGRAPHY CAT-KIT
Cardiovascular
159d
Cleared
May 16, 1985
OPTI-FLOW & OPTI-TORQUE ANGIOGRAPHIC CATHETERS
Cardiovascular
156d
Cleared
May 13, 1985
EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER
Anesthesiology
131d
Cleared
Mar 13, 1985
VAS-CATH PARALLEL DUAL LUMAN JUGULAR CANNUAL CATH
Gastroenterology & Urology
125d
Cleared
Mar 13, 1985
VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
117d
Cleared
Mar 13, 1985
VACCESS 3000 SINGLE LUMEN JUGULAR CANNULA-CATH
Gastroenterology & Urology
117d