KENLOR HUMAN SPINAL FLUID CONTROL LIQUID

KENLOR HUMAN SPINAL FLUID CONTROL LIQUID is an FDA 510(k)-cleared medical device (K890576) manufactured by Kenlor Industries, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 8, 1989. Regulation: 8.