510(k) K182518 ยท KYF Implant, Eye Valve
AHMED ClearPath Glaucoma Drainage Device
| Applicant | New World Medical, Inc., Rancho Cucamonga CA, US |
| Decision | Substantially Equivalent, Jan 18, 2019 |
| Received | Sep 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182518
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.