510(k) K090253 ยท QEZ Aspiration Thrombectomy Catheter
ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL 106552-001, ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040-001
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 8, 2009 |
| Received | Feb 2, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090253
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.