510(k) K233237 ยท GEX Powered Laser Surgical Instrument
xeo+ Family
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, Dec 15, 2023 |
| Received | Sep 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233237
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.