510(k) K243800 ยท QAI Powered Microneedle Device
PRO Pen Microneedling System (6883)
| Applicant | Dermalogica, LLC, Carson CA, US |
| Decision | Substantially Equivalent, Aug 25, 2025 |
| Received | Dec 11, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243800
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.