SENSITIVE EYES

Lens, Contact (polymethylmethacrylate)

BAUSCH & LOMB, INC.

The following data is part of a premarket notification filed by Bausch & Lomb, Inc. with the FDA for Sensitive Eyes.

Pre-market Notification Details

• Device ID: K832706
• 510k Number: K832706
• Device Name: SENSITIVE EYES
• Classification: Lens, Contact (polymethylmethacrylate)
• Applicant: BAUSCH & LOMB, 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: 1983-08-12
• Decision Date: 1983-10-04