The following data is part of a premarket notification filed by Allergan, Inc. with the FDA for Liquifilm Wetting Solution.
| Device ID | K821051 |
| 510k Number | K821051 |
| Device Name: | LIQUIFILM WETTING SOLUTION |
| Classification | Lens, Contact (polymethylmethacrylate) |
| Applicant | ALLERGAN, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | HPX |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-15 |
| Decision Date | 1982-05-13 |