510(k) K885125 ยท KYF Implant, Eye Valve
KRUPIN EYE VALVE W/SCLERAL BUCKLE
| Applicant | Hood Laboratories, Pembroke MA, US |
| Decision | Substantially Equivalent, Jan 24, 1989 |
| Received | Dec 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885125
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.