
Ams Diagnostics
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LIASYS 600 Electrolyte Measurement System, LIASYS 600 Creatinine reagent, LIASYS 600 is an FDA 510(k)-cleared medical device (K172232) manufactured by Ams Diagnostics. 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 June 11, 2019. Regulation: 8.