CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L

CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L is an FDA 510(k)-cleared medical device (K003533) manufactured by Steritec Products, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 6, 2001. Regulation: 8.