510(k) K082382 ยท QEZ Aspiration Thrombectomy Catheter
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 12, 2008 |
| Received | Aug 19, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082382
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.