PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS

PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS is an FDA 510(k)-cleared medical device (K880283) manufactured by Paceart, 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 March 8, 1988. Regulation: 8.