ABBOTT A-GENT LIQUID MAGNESIUM REAGENT, MODIFIED

ABBOTT A-GENT LIQUID MAGNESIUM REAGENT, MODIFIED is an FDA 510(k)-cleared medical device (K944202) manufactured by Abbott Laboratories. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 13, 1994. Regulation: 8.