510(k) K220032 ยท KYF Implant, Eye Valve
iStent infinite Trabecular Micro-Bypass System, Model iS3
| Applicant | Glaukos Corporation, San Clemente CA, US |
| Decision | Substantially Equivalent, Aug 2, 2022 |
| Received | Jan 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220032
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.