GAMBRO-ENGSTROM ERICA IV RESPIRATOR

GAMBRO-ENGSTROM ERICA IV RESPIRATOR is an FDA 510(k)-cleared medical device (K872482) manufactured by Gambro, 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 March 2, 1988. Regulation: 8.