
Helena Laboratories
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REP HEMOGLOBIN IEF KITS (CAT. NO. 3250) is an FDA 510(k)-cleared medical device (K901143) manufactured by Helena Laboratories. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 1990. Regulation: 8.