
Leeco Diagnostics, Inc.
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LEECO GLYCO-HEMOGLOBIN DIAGNOSTIC KIT is an FDA 510(k)-cleared medical device (K791103) manufactured by Leeco Diagnostics, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 27, 1979. Regulation: 8.