MENDEZ U/S CYSTOTOME

MENDEZ U/S CYSTOTOME is an FDA 510(k)-cleared medical device (K843386) manufactured by CooperVision, 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 November 26, 1984. Regulation: 8.