ACCUTORR V MONITOR, MODEL 0998-00-2000

ACCUTORR V MONITOR, MODEL 0998-00-2000 is an FDA 510(k)-cleared medical device (K091068) manufactured by Datascope Corp., Patient Monitoring Division. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 2009. Regulation: 8.