ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING

ACCUSTAT MODEL 102 NON-INVASIVE BLOOD MONITORING is an FDA 510(k)-cleared medical device (K881272) manufactured by Accustat, 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 June 21, 1988. Regulation: 8.