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FDA 510(k) Applications Submitted by Marijn van Stralen
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230197
01/25/2023
BoneMRI v1.6
MRIguidance B.V.
K221762
06/17/2022
BoneMRI v1.4
MRlguidance B.V.
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