DINAMAP PRO SERIES MONITOR, MODELS 110N,210N,310N,410N

DINAMAP PRO SERIES MONITOR, MODELS 110N,210N,310N,410N is an FDA 510(k)-cleared medical device (K021435) manufactured by Ge Medical Systems Information Technologies. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 2002. Regulation: 8.