KEELER CRYO MASTER & PROBES

KEELER CRYO MASTER & PROBES is an FDA 510(k)-cleared medical device (K992954) 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 December 20, 1999. Regulation: 8.