
Beckman Coulter, Inc.
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SYNCHRON LX20 CLINICAL SYSTEMS, CREATININE TEST SYSTEMS is an FDA 510(k)-cleared medical device (K071277) manufactured by Beckman Coulter, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 2007. Regulation: 8.