ULTRASPHYG BLOOD PRESSURE OPTION

ULTRASPHYG BLOOD PRESSURE OPTION is an FDA 510(k)-cleared medical device (K780046) manufactured by Cavitron Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 1978. Regulation: 8.