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: NPHERICAL AND TORIC DAILY WEAR SOFT CONTACT LENSES
• Generic Name: Lenses, soft contact, daily wear
• Regulation Number: 886.5925
• Applicant: Wavetouch Technologies, LLC; 15970 Bernardo Center Dr.; San Diego, CA 92127
• PMA Number: P860040
• Supplement Number: S002
• Date Received: 07/02/1987
• Decision Date: 05/01/1989
• Product Code: LPL
• Advisory Committee: Ophthalmic
• Supplement Type: Normal 180 Day Track
• Supplement Reason: Location Change - Manufacturer/Sterilizer/Packager/Supplier
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No