510(k) K890598 ยท KYF Implant, Eye Valve
MOLTENO IMPLANT
| Applicant | Iop, Inc., Malibu CA, US |
| Decision | Substantially Equivalent, Feb 27, 1989 |
| Received | Feb 6, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890598
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.