INTERMED, INS STERILE WATER/SALINE

INTERMED, INS STERILE WATER/SALINE is an FDA 510(k)-cleared medical device (K842166) manufactured by Intermed, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 11, 1985. Regulation: 8.