| K-number | K874657 |
| Device name | RIGID-LENS CASE |
| Applicant | Sola Ophthalmics |
| Product code | LRX |
| Device class | Class II |
| Decision date | Dec 8, 1987 |
| Decision | Substantially Equivalent |
| Regulation | 886.5928 |
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