510(k) K012852 ยท KYF Implant, Eye Valve
EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONS
| Applicant | Optonol, Ltd., Rockville MD, US |
| Decision | Substantially Equivalent, Mar 26, 2002 |
| Received | Aug 24, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012852
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.