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Orion Diagnostica, OY

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2016-03-10
TypeNumberDevice NameCodeDate
510(k) K142993 QuikRead go CRP, QuikRead go CRP Verification Set, QuikRead go CRP Control Set, and QuikRead go Instrument DCK 2016-03-10 View
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