510(k) K902491 ยท MLP Keratoprosthesis, Temporary Implant, Surgical Use
ECKHARDT TEMPORARY KERATOPROSTHESIS
| Applicant | Dutch Ophthalmic USA, Inc., Kingston NH, US |
| Decision | Substantially Equivalent, Jun 26, 1990 |
| Received | Jun 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902491
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.