ATRIAL/VENTRICULAR SEQENTIAL #080-20000

ATRIAL/VENTRICULAR SEQENTIAL #080-20000 is an FDA 510(k)-cleared medical device (K801799) manufactured by Medical Testing System, 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 January 1, 1981. Regulation: 8.