
Beckman Instruments, Inc.
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CX LIPASE REAGENT & CALIBRATOR FOR SYNCHRON CX SYSTEMS is an FDA 510(k)-cleared medical device (K952180) manufactured by Beckman Instruments, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 16, 1995. Regulation: 8.