BAXTER ADULT/PEDI INFANT SINGLE/USE MAN RESUSCIT

BAXTER ADULT/PEDI INFANT SINGLE/USE MAN RESUSCIT is an FDA 510(k)-cleared medical device (K924671) manufactured by Engineered Medical Systems. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 20, 1993. Regulation: 8.