INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE

INTERCASSETTE, INTERKIT, UNIVERSAL PAK & CASSETTE is an FDA 510(k)-cleared medical device (K890300) 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 April 16, 1989. Regulation: 8.