CRITIKON SOFT BLOOD PRESSURE CUFF

CRITIKON SOFT BLOOD PRESSURE CUFF is an FDA 510(k)-cleared medical device (K974080) manufactured by Johnson & Johnson 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 May 17, 1998. Regulation: 8.