DIGITEC TWO STAGE COMPRESSION KIT

DIGITEC TWO STAGE COMPRESSION KIT is an FDA 510(k)-cleared medical device (K993681) manufactured by Digitec Medical Service Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 20, 1999. Regulation: 8.