510(k) K112302 ยท LPL Lenses, Soft Contact, Daily Wear
PROCLEAR TORIC XR, PROCLEAR MULTIFOCAL XR, PROCLEAR MULTIFOCAL TORIC, PROCLEAR SPHERE & ASPHERE, TORIC CONTACT LENSES
| Applicant | CooperVision, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Dec 21, 2011 |
| Received | Aug 11, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112302
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.