510(k) K192138 ยท QAI Powered Microneedle Device
Rejuvapen NXT
| Applicant | Refine USA, LLC, Jacksonville Beach FL, US |
| Decision | Substantially Equivalent, Apr 9, 2020 |
| Received | Aug 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192138
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.