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 BayerLabelled 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. See the Bayer group view.
As of Nov 15, 2026, FDA's public records list Medrad Interventional (Possis Medical) with 2 510(k) clearances. The most recent is a 510(k) clearance dated Jan 21, 2011: FETCH 2 ASPIRATION CATHETER MODEL 109400-001.
| Jan 21, 2011 | FETCH 2 ASPIRATION CATHETER MODEL 109400-001K101354 · QEZ | 510(k) clearances |
| Jun 16, 2010 | ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001K101406 · QEZ | 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
