ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822

ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822 is an FDA 510(k)-cleared medical device (K014204) manufactured by K-Jump Health Co., Ltd.. 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 4, 2002. Regulation: 8.