510(k) K180778 ยท QAI Powered Microneedle Device
Exceed Microneedling Device
| Applicant | Mt. Derm GmbH, Berlin, DE |
| Decision | Substantially Equivalent, Sep 7, 2018 |
| Received | Mar 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180778
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.