510(k) K230785 ยท LPL Lenses, Soft Contact, Daily Wear
Precision1, Precision1 for Astigmatism
| Applicant | Alcon Laboratories, Inc., Fort Worth TX, US |
| Decision | Substantially Equivalent, Apr 20, 2023 |
| Received | Mar 22, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230785
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.