510(k) K030350 ยท KYF Implant, Eye Valve
EXPRESS MINI GLAUCOMA SHUNT
| Applicant | Optonol, Ltd., Duluth GA, US |
| Decision | Substantially Equivalent, Mar 13, 2003 |
| Received | Feb 3, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K030350
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.