Vas-Cath, Inc.
Vas-Cath, Inc. appears in FDA public data with 0 recalls, 27 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 19, 1998.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 27
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K973013 | OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER | June 19, 1998 |
| K965178 | NIAGARA DUAL LUMEN CATHETER | August 19, 1997 |
| K964881 | ULTRAVERSE PTA CATHETER | May 28, 1997 |
| K970725 | OPTI-PLAST XL 5.5 F PTA CATHETER | May 9, 1997 |
| K941706 | OPTI-PLAST ANGIOPLASTY CATHETER | October 18, 1994 |
| K925485 | VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETER | March 10, 1994 |
| K933483 | OPTI-PLAST 5F PTA CATHETERS | September 24, 1993 |
| K914210 | VAS-CATH DUALATOR(TM) VESSEL DILATOR | July 1, 1993 |
| K914162 | VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS | July 1, 1993 |
| K914976 | OPTI-PLAST 5F PTA CATHETERS, MODIFICATION | January 27, 1992 |
| K914500 | OPTI-PLAST 5F PTA CATHETERS, MODIFICATION | December 31, 1991 |
| K913112 | OPTI-PLAST 5F PTA CATHETERS | August 16, 1991 |
| K912984 | OPTI-PLAST 5F PTA CATHETERS, MODIFICATION | August 13, 1991 |
| K911639 | OPTI-PLAST 5F PTA CATHETERS OVEN CURING PROCEDURE | June 11, 1991 |
| K905505 | VAS-CATH URETERAL STENTS CATHETER, MODIFICATION | April 9, 1991 |
| K910996 | OPTI-PLAST 5F PTA CATHETERS | April 9, 1991 |
| K903417 | VAS-CATH OPTI-PLAST 5F PERIPHERAL ANGIOPLASTY CATH | December 5, 1990 |
| K902367 | OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETER | December 3, 1990 |
| K895597 | VAS-CATH TRIFUSION TRIPLE LUMEN INFUSION CATHETER | September 12, 1990 |
| K895506 | FLEXXICON PLUS DUAL LUMEN DIALYSIS CATHETER | February 9, 1990 |