510(k) K182902 ยท LPL Lenses, Soft Contact, Daily Wear
Precision1
| Applicant | Alcon Laboratories, Inc., Fort Worth TX, US |
| Decision | Substantially Equivalent, Dec 11, 2018 |
| Received | Oct 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182902
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 24, 2025 | Alcon Research LLC Alcon PRECISION1 One-Day Contact Lenses, -2.25D. Open, Classified |
LPL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.