The following data is part of a premarket notification filed by Allergan, Inc. with the FDA for Complete Brand Multi-purpose Solution.
| Device ID | K013479 |
| 510k Number | K013479 |
| Device Name: | COMPLETE BRAND MULTI-PURPOSE SOLUTION |
| Classification | Accessories, Soft Lens Products |
| Applicant | ALLERGAN, INC. 2525 DUPONT DR. Irvine, CA 92612 |
| Contact | Paul J Nowacki |
| Correspondent | Paul J Nowacki ALLERGAN, INC. 2525 DUPONT DR. Irvine, CA 92612 |
| Product Code | LPN |
| CFR Regulation Number | 886.5928 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-10-19 |
| Decision Date | 2002-02-11 |
| Summary: | summary |