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., part of Boston ScientificLabelled 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 15, 2026, FDA's public records list Boston Scientific/Medi-Tech with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 2002: FLEXIMA BILIARY CATHETER.
| Dec 20, 2002 | FLEXIMA BILIARY CATHETERK023870 · FGE | 510(k) clearances |
| Jan 29, 2002 | MODIFICATION TO RENEGADE FIBER BRAIDED MICROCATHETERK020012 · DQO | 510(k) clearances |
| Oct 3, 2001 | MODIFICATION TO VAXCEL DIALYSIS CATHETERK012948 · MSD | 510(k) clearances |
| Oct 2, 2001 | HEMASHIELD GOLD WOVEN DOUBLE VELOUR VASCULAR GRAFT - BRANCH GRAFTK012952 · DSY | 510(k) clearances |
| Sep 7, 2001 | IMAGER II ANGIOGRAPHIC CATHETERK011664 · DQO | 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
