MONITOR, NON-INVASIVE BLOOD PRESSURE

MONITOR, NON-INVASIVE BLOOD PRESSURE is an FDA 510(k)-cleared medical device (K782000) manufactured by Automated Screening Devices. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 4, 1978. Regulation: 8.