PROPAQ 102EL, 104EL AND 106EL

PROPAQ 102EL, 104EL AND 106EL is an FDA 510(k)-cleared medical device (K910882) 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 May 7, 1991. Regulation: 8.