510(k) K152560 ยท MMX Device, Percutaneous Retrieval
Bard Snare Retrieval Kit
| Applicant | Neometrics, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 23, 2015 |
| Received | Sep 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152560
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.