
Rapid Diagnostics, Inc.
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MICROMEDIC DRUGS OF ABUSE PANEL TEST (9), CATALOG NUMBER 07RD-7062 is an FDA 510(k)-cleared medical device (K033566) manufactured by Rapid Diagnostics, Inc.. 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 May 16, 2004. Regulation: 8.