BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF

BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFF is an FDA 510(k)-cleared medical device (K912007) manufactured by Tecnadyne Scientific, 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 July 21, 1991. Regulation: 8.