510(k) K230722 ยท HQF Laser, Ophthalmic
Eagle device
| Applicant | Belkin Vision, Ltd., Yavne, IL |
| Decision | Substantially Equivalent, Dec 8, 2023 |
| Received | Mar 16, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230722
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.