510(k) K143632 ยท LPL Lenses, Soft Contact, Daily Wear
Bausch + Lomb Biotrue ONEday for Astigmatism(nesofilcon A) Soft (hydrophilic) Contact Lens
| Applicant | Bausch & Lomb, Incorporated, Rochester NY, US |
| Decision | Substantially Equivalent, Feb 13, 2015 |
| Received | Dec 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143632
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.