510(k) K132715 ยท LPL Lenses, Soft Contact, Daily Wear
BAUSCH + LOMB BIOTURE ONEDAY FOR PRESBYOPIA (NESOFILCON A) CONTACT LENS
| Applicant | Bausch & Lomb, Incorporated, Rochester NY, US |
| Decision | Substantially Equivalent, Dec 20, 2013 |
| Received | Aug 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132715
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.