NORELCO DELUXE DIGITAL BLOOD PRESSURE

NORELCO DELUXE DIGITAL BLOOD PRESSURE is an FDA 510(k)-cleared medical device (K830685) manufactured by North American Philips Corp.. 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 17, 1983. Regulation: 8.