510(k) K110452 ยท LPL Lenses, Soft Contact, Daily Wear
SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX MTO, UNILENS 38, UNISOFT, SIMULVUE 38 LLBI 2,
| Applicant | Unilens Corp., USA, Largo FL, US |
| Decision | Substantially Equivalent, Apr 20, 2011 |
| Received | Feb 16, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110452
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.