510(k) K181230 ยท LPL Lenses, Soft Contact, Daily Wear
Largan 55 (methafilcon A) Daily Wear Soft (hydrophilic) Contact Lens, Largan 55 (methafilcon A) Daily Wear Soft (hydrophilic) Contact Lensfor ASTIGMATISM, Largan 55 (methafilcon A) Daily Wear Soft (hydrophilic) Contact Lens for PRESBYOPIA
| Applicant | Largan Medical Co., Ltd., Taichung, TW |
| Decision | Substantially Equivalent, Jun 25, 2018 |
| Received | May 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181230
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.