FUKUDA DENSHI MODEL/DS-1030A DYNASCOPE SERIES MON

FUKUDA DENSHI MODEL/DS-1030A DYNASCOPE SERIES MON is an FDA 510(k)-cleared medical device (K853213) 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 October 10, 1985. Regulation: 8.