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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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