COMPRESSAR UNIVERSAL (TM) SYSTEM

COMPRESSAR UNIVERSAL (TM) SYSTEM is an FDA 510(k)-cleared medical device (K925809) manufactured by Instromedix, 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 February 21, 1993. Regulation: 8.