Vas-Cath, Inc.
Mississauga, Ontario, CA
Vas-Cath, Inc. appears in FDA device records in Mississauga, Ontario, CA. FDA records list 27 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Vas-Cath, Inc. between 1988 and 1998. The busiest year on record is 1991, with 6. The most recent is 1998, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 3 |
| 1989 | 4 |
| 1990 | 4 |
| 1991 | 6 |
| 1992 | 1 |
| 1993 | 3 |
| 1994 | 2 |
| 1997 | 3 |
| 1998 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K973013 | OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER | LIT | Substantially Equivalent | |
| K965178 | NIAGARA DUAL LUMEN CATHETER | MPB | Substantially Equivalent | |
| K964881 | ULTRAVERSE PTA CATHETER | LIT | Substantially Equivalent | |
| K970725 | OPTI-PLAST XL 5.5 F PTA CATHETER | LIT | Substantially Equivalent | |
| K941706 | OPTI-PLAST ANGIOPLASTY CATHETER | LIT | Substantially Equivalent | |
| K925485 | VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETER | LIT | Substantially Equivalent | |
| K933483 | OPTI-PLAST 5F PTA CATHETERS | LIT | Substantially Equivalent | |
| K914210 | VAS-CATH DUALATOR(TM) VESSEL DILATOR | FKA | Substantially Equivalent | |
| K914162 | VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS | LFJ | Substantially Equivalent | |
| K914976 | OPTI-PLAST 5F PTA CATHETERS, MODIFICATION | LIT | Substantially Equivalent | |
| K914500 | OPTI-PLAST 5F PTA CATHETERS, MODIFICATION | LIT | Substantially Equivalent | |
| K913112 | OPTI-PLAST 5F PTA CATHETERS | LIT | Substantially Equivalent | |
| K912984 | OPTI-PLAST 5F PTA CATHETERS, MODIFICATION | LIT | Substantially Equivalent | |
| K911639 | OPTI-PLAST 5F PTA CATHETERS OVEN CURING PROCEDURE | LIT | Substantially Equivalent | |
| K910996 | OPTI-PLAST 5F PTA CATHETERS | LIT | Substantially Equivalent | |
| K905505 | VAS-CATH URETERAL STENTS CATHETER, MODIFICATION | FAD | Substantially Equivalent | |
| K903417 | VAS-CATH OPTI-PLAST 5F PERIPHERAL ANGIOPLASTY CATH | LIT | Substantially Equivalent | |
| K902367 | OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER | LIT | Substantially Equivalent | |
| K895597 | VAS-CATH TRIFUSION TRIPLE LUMEN INFUSION CATHETER | FOZ | Substantially Equivalent | |
| K895506 | FLEXXICON PLUS DUAL LUMEN DIALYSIS CATHETER | LFJ | Substantially Equivalent | |
| K892926 | DUAL LUMEN CATHETER FOR CHRONIC VASCULAR ACCESS | LJS | Substantially Equivalent | |
| K894357 | VAS-CATH URETERAL STENT CATHETER | FAD | Substantially Equivalent | |
| K890099 | MODIFIED VAS-CATH CATHETER REPAIR KIT | LFJ | Substantially Equivalent | |
| K890717 | MODIFICATION HEMOFILTRATION CATHETER HF-100 | LFK | Substantially Equivalent | |
| K883768 | VAS-CATH CATHETER REPAIR KIT | LFJ | Substantially Equivalent | |
| K882466 | VAS-CATH PEDIATRIC HEMOFILTRATION CATHETER | LFK | Substantially Equivalent | |
| K881743 | VAS-CATH FLEXXICON DUAL LUMEN DIALYSIS CATHETER | LFJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- LITCatheter, Angioplasty, Peripheral, Transluminal
- LFKCatheter, Femoral
- MPBCatheter, Hemodialysis, Non-Implanted
- LJSCatheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- LFJCatheter, Subclavian
- FKADilator, Vessel
- FADStent, Ureteral
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain