510(k) K182304 ยท HQD Lens, Contact (Other Material) - Daily
Hyper GP (tisilfocon A) Daily Wear Contact Lens
| Applicant | Contamac, Ltd., Saffron Walden, GB |
| Decision | Substantially Equivalent, Nov 23, 2018 |
| Received | Aug 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182304
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.