510(k) K231011 ยท HQF Laser, Ophthalmic
Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse
| Applicant | Meridian AG, Thun, CH |
| Decision | Substantially Equivalent, Sep 12, 2023 |
| Received | Apr 10, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231011
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.