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Ikonisys, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080909 ICONOSCOPE ONCOFISH HER2 TEST SYSTEM, MODEL 2000NTH2008-10-17 View
510(k) K062755 IKONISCOPE ONCOFISH BLADDER TEST SYSTEMJOY2007-01-04 View
510(k) K061392 IKONISCOPE FASTFISH AUTO/AMNIOCYTE TEST SYSTEMJOY2006-08-01 View
510(k) K052577 IKONISCOPE FASTFISH AMNIO IMAGING SYSTEMJOY2006-01-24 View
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