LAERDAL(TM) POCKET MASK, MODIFICATION

LAERDAL(TM) POCKET MASK, MODIFICATION is an FDA 510(k)-cleared medical device (K933048) manufactured by Laerdal Medical Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 1, 1993. Regulation: 8.