WELCH ALLYN DURASHOCK BLOOD PRESSURE SYSTEM

WELCH ALLYN DURASHOCK BLOOD PRESSURE SYSTEM is an FDA 510(k)-cleared medical device (K012455) manufactured by Welch Allyn, 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 August 16, 2001. Regulation: 8.