Vascutech, Inc.
Vascutech, Inc. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 6, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K001621 | DARDIK CAROTID SHUNT | December 6, 2000 |
| K992942 | LEMAITRE OCCLUSION CATHETER | April 13, 2000 |
| K992933 | LEMAITRE IRRIGATION CATHETER | March 8, 2000 |
| K992934 | LEMAITRE VENOUS THROMBECTOMY CATHETER | March 1, 2000 |
| K992940 | LEMAITRE BALLOON CATHETER WITH IRRIGATION | February 22, 2000 |
| K992941 | LEMAITRE BILIARY CATHETER | January 12, 2000 |
| K992368 | LEMAITRE EMBOLECTOMY CATHETER | December 9, 1999 |
| K980723 | 2.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT) | February 12, 1999 |
| K946352 | LEMAITRE VALVULOTOME II | June 21, 1995 |
| K932009 | THE SAMUELS RETROGRAD VALVULOTOME | September 21, 1993 |
| K932184 | STERILE LEMAITRE GLOW 'N TELL TAPE | July 22, 1993 |
| K924171 | LEMAITRE RETROGRADE VALVULOTOME | February 16, 1993 |
| K912548 | LEMAITRE-BOOKWALTER VESSEL DEVICES | September 18, 1991 |
| K850394 | LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTR | April 24, 1985 |