DINAMAP PLUS VITAL SIGNS MONOITOR

DINAMAP PLUS VITAL SIGNS MONOITOR is an FDA 510(k)-cleared medical device (K943709) manufactured by Critikon Company, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 1995. Regulation: 8.