510(k) K152335 ยท DXE Catheter, Embolectomy
Export Advance Aspiration Catheter
| Applicant | Medtronic, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Sep 18, 2015 |
| Received | Aug 19, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152335
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.