LARYNGOSCOPE BLADE (ROBERTSHAW STYLE)

LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) is an FDA 510(k)-cleared medical device (K884073) manufactured by Eastmed Enterprises, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 12, 1988. Regulation: 8.