510(k) K062252 ยท KYF Implant, Eye Valve
MOLTENO3
| Applicant | Iop, Inc., Costa Mesa CA, US |
| Decision | Substantially Equivalent, Sep 27, 2006 |
| Received | Aug 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062252
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 22, 2016 | Innovative Ophthalmic Products, Inc Molteno3 Glaucoma Implants G-Series:
GS-Single Plate 175mm2 (IOP reorder#: M3-175)
GL-Single Plate 230mm2 (IOP reorder#: M3-230) Terminated |
KYF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.