LINDLEY II RESUSCITATOR

LINDLEY II RESUSCITATOR is an FDA 510(k)-cleared medical device (K881689) manufactured by Lindley Resuscitator, 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 7, 1988. Regulation: 8.