510(k) K840204 ยท KYF Implant, Eye Valve
WHITE OCULAR PRESSURE RELIEF DEVICE
| Applicant | Precision-Cosmet Co., Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Feb 15, 1985 |
| Received | Jan 19, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840204
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.