510(k) K170358 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
joimax Endovapor 2
| Applicant | Joimax GmbH, Karlsruhe, DE |
| Decision | Substantially Equivalent, Apr 21, 2017 |
| Received | Feb 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170358
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.