510(k) K133629 ยท QEW Peripheral Mechanical Thrombectomy With Aspiration
ANGIOJET ULTRA AVX THROMBECTOMY SET
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 14, 2014 |
| Received | Nov 26, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133629
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 13, 2015 | Boston Scientific Corporation AngioJet AVX Thrombectomy Set: UPN 105039-001, Catalog No.105039, Sterilized Using Ethylene Oxide. For breaking apart and removing thrombus from vascul Terminated |
DXE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.