FUKUDA DENSHI MODEL HJ-310

FUKUDA DENSHI MODEL HJ-310 is an FDA 510(k)-cleared medical device (K901889) manufactured by Fukuda Denshi USA, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 1990. Regulation: 8.