LDH-L LIQUID ENZYMATIC, KINETIC KIT

LDH-L LIQUID ENZYMATIC, KINETIC KIT is an FDA 510(k)-cleared medical device (K810083) manufactured by Bio-Analytics Laboratories, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 1981. Regulation: 8.