JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER

JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER is an FDA 510(k)-cleared medical device (K872917) manufactured by American Pharmaseal Div. Ahsc. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 10, 1987. Regulation: 8.