REACTIFS, IBF ULTROGELS ACA & ULTROGELS A

REACTIFS, IBF ULTROGELS ACA & ULTROGELS A is an FDA 510(k)-cleared medical device (K844164) manufactured by Lkb Instruments, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 9, 1984. Regulation: 8.