Premarket Approval (PMA)

Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.

• Device: 3M VISION CARE POSTERIOR CHAMBER IOL,PERSPEX CQ-UV
• Generic Name: intraocular lens
• Regulation Number: 886.3600
• Applicant: Alcon Research, Ltd.; 6201 S. Fwy.; Fort Worth, TX 76134
• PMA Number: P830040
• Supplement Number: S023
• Date Received: 10/01/1991
• Decision Date: 10/17/1991
• Withdrawal Date: 06/23/2010
• Product Code: HQL
• Advisory Committee: Ophthalmic
• Supplement Type: Normal 180 Day Track
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No