510(k) K183200 ยท MUW Lens, Contact (Orthokeratology)
iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses
| Applicant | C&E GP Specialist, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 9, 2019 |
| Received | Nov 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183200
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.