CK 6000 SERIES, TOWELS

CK 6000 SERIES, TOWELS is an FDA 510(k)-cleared medical device (K864697) 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 17, 1986. Regulation: 8.