PRE-SERT
Lens, Contact (polymethylmethacrylate)
ALLERGAN, INC.
The following data is part of a premarket notification filed by Allergan, Inc. with the FDA for Pre-sert.
Pre-market Notification Details
| Device ID | K822706 |
| 510k Number | K822706 |
| Device Name: | PRE-SERT |
| 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 | 1982-09-07 |
| Decision Date | 1982-10-22 |
Trademark Results [PRE-SERT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PRE-SERT 72418897 0962489 Dead/Expired |
ALLERGAN PHARMACEUTICALS 1972-03-20 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.