Vas-Cath of Canada , Ltd.
Vas-Cath of Canada , Ltd. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1988.
Top product codes for Vas-Cath of Canada , Ltd.
Recent clearances by Vas-Cath of Canada , Ltd.
- K875188 — LUER LOCK CONNECTORS / RIDIG P.V.C.
- K871817 — VAS-CATH PERITONEAL DIALYSIS CATHETER
- K871487 — VAS-CATH PERMANENT SINGLE LUMEN HEMODIALYSIS CATH
- K871488 — VAS-CATH PERMANENT DUAL LUMEN HEMODIALYSIS CATH
- K863982 — VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAY
- K853283 — VACCESS TM 4006
- K844854 — OPTI-FLOW DIGITAL SUBTRACTION ANGIOGRAPHY CAT-KIT
- K844800 — OPTI-FLOW & OPTI-TORQUE ANGIOGRAPHIC CATHETERS
- K850009 — EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETER
- K844336 — VAS-CATH PARALLEL DUAL LUMAN JUGULAR CANNUAL CATH
- K844433 — VACCESS 2000 SINGLE LUMEN SUBCLAVIAN CANNULA
- K844434 — VACCESS 3000 SINGLE LUMEN JUGULAR CANNULA-CATH
- K844982 — VAS-CATH CONTINOUS EPIDURAL ANESTH. CATH/KIT/TRAY
- K842864 — VACCESS FEMORAL CANNULA
- K834232 — VAS-CATH DSA CATHETER/TRAY
- K840322 — HEMOFILTRATION CATHETER HF-100
- K834358 — PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA
- K810745 — DOUBLE LUMEN SUBCLAVIN CATHETER SC-400
- K791308 — ULDALL SUBCLAVIAN CANNULA SC-100
Data sourced from openFDA. This site is unofficial and independent of the FDA.