AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600

AMPLIEF WRIST BLOOD PRESSURE MONITOR, MODEL M600 is an FDA 510(k)-cleared medical device (K050413) manufactured by Amplife Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 3, 2005. Regulation: 8.