Largan Medical Co., Ltd. · Class II · Cleared Nov 1, 2018
| K-number | K182523 |
| Device name | Largan 55 UV Color (Ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens |
| Applicant | Largan Medical Co., Ltd. |
| Product code | LPL |
| Device class | Class II |
| Decision date | Nov 1, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 886.5925 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov