
Diagnostic Products Corp.
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IMMULITE METHAMPHETAMINE, MODEL LKMA1, LKMA5 is an FDA 510(k)-cleared medical device (K992634) manufactured by Diagnostic Products Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 19, 2000. Regulation: 8.