ELECTRONIC BLOOD PRESS. METER EN-212

ELECTRONIC BLOOD PRESS. METER EN-212 is an FDA 510(k)-cleared medical device (K832076) manufactured by Panasonic Co. Div. Matsu Elec. Corp. America. 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 25, 1984. Regulation: 8.