
Boehringer Mannheim Corp.
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CEDIA DAU MULTI-DRUG CONTROL CEDIA DAU SPECIALTY CONTROL SET 1 is an FDA 510(k)-cleared medical device (K965157) manufactured by Boehringer Mannheim Corp.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 16, 1997. Regulation: 8.