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 |