510(k) K172314 ยท HQD Lens, Contact (Other Material) - Daily
Ampleye Scleral RGP Lens (roflufocon D, roflufocon E, hexafocon A, paflufocon D)
| Applicant | Art Optical Contact Lens, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Sep 20, 2017 |
| Received | Aug 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172314
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.