PROPAQ 102,104,106,102EL,104EL,&106EL

PROPAQ 102,104,106,102EL,104EL,&106EL is an FDA 510(k)-cleared medical device (K914838) manufactured by Protocol Systems, 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 9, 1992. Regulation: 8.