CK 4900 SERIES, GOWN AND TOWEL PAK

CK 4900 SERIES, GOWN AND TOWEL PAK is an FDA 510(k)-cleared medical device (K874760) manufactured by Currie Medical Specialties, 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 December 9, 1987. Regulation: 8.