PATIENT MON 1280/1281/120C/121C & MULTI-PARA CART

PATIENT MON 1280/1281/120C/121C & MULTI-PARA CART is an FDA 510(k)-cleared medical device (K860646) manufactured by Analogic Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 15, 1986. Regulation: 8.