OLYMPUS INORGANIC PHOSPHORUS (2-REAGENT MODIFICA.)

OLYMPUS INORGANIC PHOSPHORUS (2-REAGENT MODIFICA.) is an FDA 510(k)-cleared medical device (K901807) manufactured by Em Diagnostic Systems, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 1, 1990. Regulation: 8.