MOBAY (BAYER) MERLON M-40 (H)F 1112

MOBAY (BAYER) MERLON M-40 (H)F 1112 is an FDA 510(k)-cleared medical device (K873822) manufactured by Applied Laboratories, 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 March 23, 1988. Regulation: 8.