CARDIOTOMY RESERVOIR W/20 MICRON FILITER

CARDIOTOMY RESERVOIR W/20 MICRON FILITER is an FDA 510(k)-cleared medical device (K920178) manufactured by Lifestream Int'L, 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 12, 1993. Regulation: 8.