FDA 510(k) Applications for Medical Device Product Code "QPS"

FDA 510(k) Number Applicant Device Name Decision Date
K213936 DiaSorin Inc. LIAISON MeMed BV, LIAISON MeMed BV Control Set 07/14/2022
K230944 MeMed Diagnostics Ltd. MeMed BV 06/30/2023
K210254 MeMed Diagnostics Ltd. MeMed BV 09/01/2021
K222332 MeMed Diagnostics Ltd. MeMed BV 03/23/2023


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