510(k) K172014 ยท DQY Catheter, Percutaneous
Wedge Microcatheter
| Applicant | MicroVention, Inc., Tistin CA, US |
| Decision | Substantially Equivalent, Apr 5, 2018 |
| Received | Jul 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172014
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.