IMPRAFLO AUTOTRANSFUSION DEVICE

IMPRAFLO AUTOTRANSFUSION DEVICE is an FDA 510(k)-cleared medical device (K901232) manufactured by Impra, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 17, 1990. Regulation: 8.