LEWICKY ANTERIOR CHAMBER MAINTEN. SYS.

LEWICKY ANTERIOR CHAMBER MAINTEN. SYS. is an FDA 510(k)-cleared medical device (K802381) manufactured by Fibra Sonics, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1980. Regulation: 8.