ALL PURPOSE CUFF, MODEL 222APC

ALL PURPOSE CUFF, MODEL 222APC is an FDA 510(k)-cleared medical device (K051904) manufactured by Suntech Medical, 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 September 8, 2005. Regulation: 8.