510(k) K163524 ยท DWP Dilator, Vessel, Surgical
Vessel Dilator
| Applicant | Fetzer Medical GmbH & Co. KG, Tuttlingen, DE |
| Decision | Substantially Equivalent, Jun 29, 2017 |
| Received | Dec 15, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163524
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.