510(k) K182674 ยท LPL Lenses, Soft Contact, Daily Wear
Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens, Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens for Astigmatism, Largan U38 (Polymacon) Daily Wear Soft (hydrophilic) Contact Lens for Presbyopia
| Applicant | Largan Medical Co., Ltd., Taichung, TW |
| Decision | Substantially Equivalent, Nov 13, 2018 |
| Received | Sep 26, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182674
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.