510(k) K213592 ยท HQF Laser, Ophthalmic
Iridex 810 Laser
| Applicant | Iridex Corporation, Mountain View CA, US |
| Decision | Substantially Equivalent, Mar 23, 2022 |
| Received | Nov 12, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213592
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.