
Beckman Coulter, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO SYNCHRON LX CLINICAL CHEMISTRY SYSTEMS (LX20 AND LX20 PRO) is an FDA 510(k)-cleared medical device (K014034) 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 December 17, 2001. Regulation: 8.