Medical Device Manufacturer · CA , Mississauga, Ontario

Vas-Cath, Inc. - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 1988

Total

Cleared

Denied

Vas-Cath, Inc. has 27 FDA 510(k) cleared medical devices. Based in Mississauga, Ontario, CA.

Historical record: 27 cleared submissions from 1988 to 1998. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Vas-Cath, Inc. Filter by specialty or product code using the sidebar.

Vas-Cath, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vas-Cath, Inc.

27 devices

1-12 of 27

Cleared Jun 19, 1998

OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER

K973013 · LIT

Cardiovascular · 310d

Cleared Aug 19, 1997

NIAGARA DUAL LUMEN CATHETER

K965178 · MPB

Gastroenterology & Urology · 238d

Cleared May 28, 1997

ULTRAVERSE PTA CATHETER

K964881 · LIT

Cardiovascular · 174d

Cleared May 09, 1997

OPTI-PLAST XL 5.5 F PTA CATHETER

K970725 · LIT

Cardiovascular · 70d

Cleared Oct 18, 1994

OPTI-PLAST ANGIOPLASTY CATHETER

K941706 · LIT

Cardiovascular · 195d

Cleared Mar 10, 1994

VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETER

K925485 · LIT

Cardiovascular · 496d

Cleared Sep 24, 1993

OPTI-PLAST 5F PTA CATHETERS

K933483 · LIT

Cardiovascular · 86d

Cleared Jul 01, 1993

VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS

K914162 · LFJ

Gastroenterology & Urology · 653d

Cleared Jul 01, 1993

VAS-CATH DUALATOR(TM) VESSEL DILATOR

K914210 · FKA

Gastroenterology & Urology · 651d

Cleared Jan 27, 1992

OPTI-PLAST 5F PTA CATHETERS, MODIFICATION

K914976 · LIT

Cardiovascular · 82d

Cleared Dec 31, 1991

OPTI-PLAST 5F PTA CATHETERS, MODIFICATION

K914500 · LIT

Cardiovascular · 84d

Cleared Aug 16, 1991

OPTI-PLAST 5F PTA CATHETERS

K913112 · LIT

Cardiovascular · 42d

Vas-Cath, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Vas-Cath, Inc.

Filters