MODEL DS-504 DYNASCOPE PATIENT MONITOR

MODEL DS-504 DYNASCOPE PATIENT MONITOR is an FDA 510(k)-cleared medical device (K893405) 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 1, 1989. Regulation: 8.