Acrysof (R) UV Absorbing Intraocular Lenses

FDA premarket approval P930014 · intraocular lens

PMA numberP930014

Approval

Applicant
Alcon Laboratories, Inc.
Received
May 28, 1993
Decision date
December 22, 1994 (APPR)
Supplements
161, latest July 8, 2026
Product code
HQL – Intraocular Lens

Official FDA PMA record

Approval order statement

Approval for the ACRYSOf® Models MA60BM and MA30BA Ultraviolet-Absorbing Acrylic Foldable UV-Absorbing Posterior Chamber Intraocular Lenses (IOLs). These devices are indicated for replacement of the human lens to achieve visual correction of aphakia in patients 60 years of age and older when extracapsular cataract extraction or phacoemulsification are performed. These lenses are intended for placement in the capsular bag.