KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT)

KEELER APPLANATION TONOMETER; T-TYPE KAT, K-TYPE KAT, (KAT) is an FDA 510(k)-cleared medical device (K093445) manufactured by Keeler, Ltd.. 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 18, 2010. Regulation: 8.