510(k) K233304 ยท GEX Powered Laser Surgical Instrument
Omnimax S3, Omnimax S4
| Applicant | Sharplight Technologies, Ltd., Rishon Le Zion, IL |
| Decision | Substantially Equivalent, Dec 22, 2023 |
| Received | Sep 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233304
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.