510(k) K160938 ยท HQD Lens, Contact (Other Material) - Daily
SynergEyes SiH with Hydra-PEG(petrafocon A hem-larafilcon A) Hybrid Daily Wear Lens
| Applicant | Synergeyes, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 1, 2016 |
| Received | Apr 4, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160938
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.