Largan Medical Co., Ltd. · Class II · Cleared Jun 29, 2018
| K-number | K181232 |
| Device name | Largan 55 UV (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens, Largan 55 UV (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens for Astigmatism, Largan 55 UV (ocufilcon D) Daily Wear Soft (hydrophilic) Contact Lens for Presbyopia |
| Applicant | Largan Medical Co., Ltd. |
| Product code | LPL |
| Device class | Class II |
| Decision date | Jun 29, 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