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Allergan, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest Approval2019-08-08
TypeNumberDevice NameCodeDate
510(k) K190674 REFRESH RELIEVA For CONTACTS LPN 2019-08-08 View
510(k) K161457 XEN Glaucoma Treatment System KYF 2016-11-21 View