Vas-Cath, Inc.
Vas-Cath, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1998.
Top product codes for Vas-Cath, Inc.
Recent clearances by Vas-Cath, Inc.
- K973013 — OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER
- K965178 — NIAGARA DUAL LUMEN CATHETER
- K964881 — ULTRAVERSE PTA CATHETER
- K970725 — OPTI-PLAST XL 5.5 F PTA CATHETER
- K941706 — OPTI-PLAST ANGIOPLASTY CATHETER
- K925485 — VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETER
- K933483 — OPTI-PLAST 5F PTA CATHETERS
- K914162 — VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS
- K914210 — VAS-CATH DUALATOR(TM) VESSEL DILATOR
- K914976 — OPTI-PLAST 5F PTA CATHETERS, MODIFICATION
- K914500 — OPTI-PLAST 5F PTA CATHETERS, MODIFICATION
- K913112 — OPTI-PLAST 5F PTA CATHETERS
- K912984 — OPTI-PLAST 5F PTA CATHETERS, MODIFICATION
- K911639 — OPTI-PLAST 5F PTA CATHETERS OVEN CURING PROCEDURE
- K905505 — VAS-CATH URETERAL STENTS CATHETER, MODIFICATION
- K910996 — OPTI-PLAST 5F PTA CATHETERS
- K903417 — VAS-CATH OPTI-PLAST 5F PERIPHERAL ANGIOPLASTY CATH
- K902367 — OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER
- K895597 — VAS-CATH TRIFUSION TRIPLE LUMEN INFUSION CATHETER
- K895506 — FLEXXICON PLUS DUAL LUMEN DIALYSIS CATHETER
- K892926 — DUAL LUMEN CATHETER FOR CHRONIC VASCULAR ACCESS
- K894357 — VAS-CATH URETERAL STENT CATHETER
- K890099 — MODIFIED VAS-CATH CATHETER REPAIR KIT
- K890717 — MODIFICATION HEMOFILTRATION CATHETER HF-100
- K883768 — VAS-CATH CATHETER REPAIR KIT
- K882466 — VAS-CATH PEDIATRIC HEMOFILTRATION CATHETER
- K881743 — VAS-CATH FLEXXICON DUAL LUMEN DIALYSIS CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.