510(k) K232273 ยท HLZ Electrode, Corneal
RM Electrode (RMH 23-01)
| Applicant | Retmap, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Dec 7, 2023 |
| Received | Jul 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232273
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.