510(k) K163307 ยท MMX Device, Percutaneous Retrieval
Expro Elite Snare, Sympro Elite Snare
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 8, 2017 |
| Received | Nov 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163307
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.