TYCOS SELF CHECK BPM3 BLOOD PRESS MONI

TYCOS SELF CHECK BPM3 BLOOD PRESS MONI is an FDA 510(k)-cleared medical device (K840469) manufactured by Sybron 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 May 20, 1984. Regulation: 8.