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Alicia Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K925909 GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATIONGKZ1994-10-27 View
510(k) K910679 GENESIS I AUTOMATED CELL COUNTERGKL1991-05-07 View
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