510(k) K233709 ยท QAI Powered Microneedle Device
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| Applicant | Mt. Derm GmbH, Berlin, DE |
| Decision | Substantially Equivalent, Feb 23, 2024 |
| Received | Nov 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233709
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.