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: THE AMCON WAY II
• Generic Name: Accessories, soft lens products
• Regulation Number: 886.5928
• Applicant: Amcon, Inc.; 1102 Main St.; P.O. Box 176; Grandview, MO 64030
• PMA Number: P800069
• Supplement Number: S004
• Date Received: 05/12/1982
• Decision Date: 02/28/1983
• Product Code: LPN
• Advisory Committee: Ophthalmic
• Expedited Review Granted?: No
• Combination Product: No
• Predetermined Change Control Plan Authorized: No