The following data is part of a premarket notification filed by Allergan Optical with the FDA for Allergan Lens Case.
| Device ID | K884251 |
| 510k Number | K884251 |
| Device Name: | ALLERGAN LENS CASE |
| Classification | Case, Contact Lens |
| Applicant | ALLERGAN OPTICAL 2525 DUPONT DR. P.O. BOX 19534 Irvine, CA 92623 -9534 |
| Contact | Takruri, Phd |
| Correspondent | Takruri, Phd ALLERGAN OPTICAL 2525 DUPONT DR. P.O. BOX 19534 Irvine, CA 92623 -9534 |
| Product Code | LRX |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-10-11 |
| Decision Date | 1988-12-28 |