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 Angeion Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 18, 1993: ANGEION IGITAL ANGEFLATOR.
| Date | Record | Source |
|---|---|---|
| Mar 18, 1993 | ANGEION IGITAL ANGEFLATORK921757 · MAV | 510(k) clearances |
| Jan 12, 1993 | ANGESTAT(R) PERICARDIAL DRAINAGE SHEATH SETK925533 · GBX | 510(k) clearances |
| Feb 18, 1992 | ANGEION ENDOSCOPIC VALVE SEALK915719 · ODC | 510(k) clearances |
| Dec 13, 1990 | ANGEFLATOR(TM)K902377 · DXT | 510(k) clearances |
| Apr 30, 1990 | Y-ADAPTER W/THOUY BORSTK895580 · DYB | 510(k) clearances |
| Nov 30, 1989 | ANGEION HEMOSTASIS VALVE INTRODUCERK894446 · DYB | 510(k) clearances |
| Jun 24, 1987 | CATHETER INTRODUCERK871153 · DYB | 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
