Vas-Cath of Canada , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LUER LOCK CONNECTORS / RIDIG P.V.C., VAS-CATH PERITONEAL DIALYSIS CATHETER, VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH
19
Total
19
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vas-Cath of Canada , Ltd. Gastroenterology & Urology ✕
13 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
Aug 22, 1985
VACCESS TM 4006
Gastroenterology & Urology
17d
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
Cleared
Aug 08, 1984
VACCESS FEMORAL CANNULA
Gastroenterology & Urology
16d
Cleared
Apr 24, 1984
HEMOFILTRATION CATHETER HF-100
Gastroenterology & Urology
90d
Cleared
Apr 02, 1984
PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA
Gastroenterology & Urology
111d
Cleared
Mar 31, 1981
DOUBLE LUMEN SUBCLAVIN CATHETER SC-400
Gastroenterology & Urology
12d
Cleared
Aug 03, 1979
ULDALL SUBCLAVIAN CANNULA SC-100
Gastroenterology & Urology
18d