510(k) K895013 ยท MLP Keratoprosthesis, Temporary Implant, Surgical Use
COBO TEMPORARY KERATOPROSTHESIS
| Applicant | Ocular Instruments, Inc., Bellevue WA, US |
| Decision | Substantially Equivalent, Oct 31, 1989 |
| Received | Aug 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895013
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.