510(k) K221759 ยท LYX Media, Corneal Storage
Cornisol
| Applicant | Aurolab, Veerapanjan, Madurai, IN |
| Decision | Substantially Equivalent, Oct 5, 2022 |
| Received | Jun 17, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221759
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.