Katalyst Cyclophotocoagulation Probe

Katalyst Cyclophotocoagulation Probe is an FDA 510(k)-cleared medical device (K163632) manufactured by Katalyst Surgical, LLC. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 14, 2017. Regulation: 8.