510(k) K221070 ยท QAI Powered Microneedle Device
DP4 Microneedling device
| Applicant | Equipmed USA, LLC, Newport Beach CA, US |
| Decision | Substantially Equivalent, Dec 20, 2022 |
| Received | Apr 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221070
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.