
Polymedica Pharmaceuticals, U.S.A., Inc.]
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LIBERTY BLOOD GLUCOSE MONITORING SYSTEM is an FDA 510(k)-cleared medical device (K014167) manufactured by Polymedica Pharmaceuticals, U.S.A., 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 February 18, 2002. Regulation: 8.