The following data is part of a premarket notification filed by Allergan, Inc. with the FDA for Soakare.
| Device ID | K821052 |
| 510k Number | K821052 |
| Device Name: | SOAKARE |
| Classification | Lens, Contact (polymethylmethacrylate) |
| Applicant | ALLERGAN, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| 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 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SOAKARE 74050913 not registered Dead/Abandoned |
Allergan, Inc. 1990-04-20 |
![]() SOAKARE 73043686 1029863 Dead/Expired |
ALLERGAN PHARMACEUTICALS 1975-02-07 |
![]() SOAKARE 72273454 0851799 Dead/Expired |
ALLERGAN PHARMACEUTICALS 1967-06-09 |