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 MedtronicLabelled 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 Possis Medical with 34 510(k) clearances. The most recent is a 510(k) clearance dated Feb 14, 2014: ANGIOJET ULTRA AVX THROMBECTOMY SET.
| Feb 14, 2014 | ANGIOJET ULTRA AVX THROMBECTOMY SETK133629 · QEW | 510(k) clearances |
| Jun 22, 2009 | ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETSK091593 · QEZ | 510(k) clearances |
| Apr 8, 2009 | ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL 106552-001, ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040-001K090253 · QEZ | 510(k) clearances |
| Dec 12, 2008 | ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039K082382 · QEZ | 510(k) clearances |
| Sep 26, 2008 | MODIFICATION TO FETCH ASPIRATION CATHETERK081989 · QEZ | 510(k) clearances |
| Jun 13, 2008 | GUARDDOG OCCLUSION GUIDEWIRE, INFLATION DEVICEK081454 · MJN | 510(k) clearances |
| Apr 4, 2008 | ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608K080806 · QEZ | 510(k) clearances |
| Jan 24, 2008 | ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039K073441 · 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
