VITALOGRAPH 2110 SOFTWARE INTERFACE

VITALOGRAPH 2110 SOFTWARE INTERFACE is an FDA 510(k)-cleared medical device (K950854) manufactured by Vitalograph , Ltd.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 11, 1995. Regulation: 8.