KATALYST LASER PROBES, KATALYST ILLUMINATED LASER PROBES

KATALYST LASER PROBES, KATALYST ILLUMINATED LASER PROBES is an FDA 510(k)-cleared medical device (K121187) 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 September 16, 2012. Regulation: 8.