Allergan, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2019-08-08
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K190674 | REFRESH RELIEVA For CONTACTS | LPN | 2019-08-08 | View |
| 510(k) | K161457 | XEN Glaucoma Treatment System | KYF | 2016-11-21 | View |
No matching devices.