Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Vascutech with 14 510(k) clearances. The most recent is a 510(k) clearance dated Dec 6, 2000: DARDIK CAROTID SHUNT.
| Date | Record | Source |
|---|---|---|
| Dec 6, 2000 | DARDIK CAROTID SHUNTK001621 · MJN | 510(k) clearances |
| Apr 13, 2000 | LEMAITRE OCCLUSION CATHETERK992942 · MJN | 510(k) clearances |
| Mar 8, 2000 | LEMAITRE IRRIGATION CATHETERK992933 · DXE | 510(k) clearances |
| Mar 1, 2000 | LEMAITRE VENOUS THROMBECTOMY CATHETERK992934 · DXE | 510(k) clearances |
| Feb 22, 2000 | LEMAITRE BALLOON CATHETER WITH IRRIGATIONK992940 · DXE | 510(k) clearances |
| Jan 12, 2000 | LEMAITRE BILIARY CATHETERK992941 · LQR | 510(k) clearances |
| Dec 9, 1999 | LEMAITRE EMBOLECTOMY CATHETERK992368 · DXE | 510(k) clearances |
| Feb 12, 1999 | 2.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT)K980723 · MGZ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
