510(k) K232657 ยท EKX Handpiece, Direct Drive, Ac-Powered
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| Applicant | Perimetrics, Inc., Newport Beach CA, US |
| Decision | Substantially Equivalent, Sep 1, 2023 |
| Received | Aug 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232657
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.