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Mriguidance B.V.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K233030
BoneMRI
March 1, 2024
K230197
BoneMRI v1.6
February 22, 2023
K202404
BoneMRI
December 22, 2021