
Alicia Diagnostics, Inc.
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GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION is an FDA 510(k)-cleared medical device (K925909) manufactured by Alicia 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 October 26, 1994. Regulation: 8.