510(k) K230228 ยท HQF Laser, Ophthalmic
Iridex 532 Laser; Iridex 577 Laser; Iridex Laser (532 nm and 577 nm models)
| Applicant | Iridex Corporation, Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 23, 2023 |
| Received | Jan 27, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230228
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.