PMA P060022S020

Device: AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
Applicant: Bausch & Lomb, Inc.
PMA number: P060022
Supplement: S020
Product code: HQL
Decision date: 2015-02-03
Generic name: intraocular lens
Approval order statement: APPROVAL TO MODIFY THE LABELING TO INCLUDE THE BAUSCH + LOMB IOLINJECTOR (MODEL VIS100) TO THE VALIDATED INSERTERS LIST ON THE LABELING OF THE AKREOS AO60 INTRAOCULAR LENS (IOL).

Current openFDA PMA Record#

Device: AKREOS POSTERIOR CHAMBER INTRAOCULAR LENS
Applicant: Bausch & Lomb, Inc.
PMA number: P060022
Supplement: S020
Product code: HQL
Generic name: intraocular lens
Decision date: 2015-02-03
Decision code: APPR
Date received: 2014-12-08
Supplement type: Real-Time Process
Supplement reason: Change Design/Components/Specifications/Material
Approval order statement: APPROVAL TO MODIFY THE LABELING TO INCLUDE THE BAUSCH + LOMB IOLINJECTOR (MODEL VIS100) TO THE VALIDATED INSERTERS LIST ON THE LABELING OF THE AKREOS AO60 INTRAOCULAR LENS (IOL).