KEELER ACU 22XT OPHTHALMIC CRYO UNIT

KEELER ACU 22XT OPHTHALMIC CRYO UNIT is an FDA 510(k)-cleared medical device (K874555) manufactured by Keeler Instruments, 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 January 28, 1988. Regulation: 8.