MODEL C2100-SERIES OPHTHALMIC CRYOPROBE

MODEL C2100-SERIES OPHTHALMIC CRYOPROBE is an FDA 510(k)-cleared medical device (K810409) manufactured by Valleylab, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 1981. Regulation: 8.