510(k) K233803 ยท GEX Powered Laser Surgical Instrument
UltraClear Laser System (N/A)
| Applicant | Acclaro Corporation, Smithfield RI, US |
| Decision | Substantially Equivalent, May 8, 2024 |
| Received | Nov 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233803
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.