TOTAL

Lens, Contact (polymethylmethacrylate)

ALLERGAN, INC.

The following data is part of a premarket notification filed by Allergan, Inc. with the FDA for Total.

Pre-market Notification Details

• Device ID: K821054
• 510k Number: K821054
• Device Name: TOTAL
• Classification: Lens, Contact (polymethylmethacrylate)
• Applicant: ALLERGAN, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: HPX
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1982-04-15
• Decision Date: 1982-05-13