
Clinical Controls, Inc.
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CARDIOSPEX(TM) LIQUID CKMB/LD-1 IMMUNOINHIBITION is an FDA 510(k)-cleared medical device (K946146) manufactured by Clinical Controls, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 23, 1995. Regulation: 8.