Mrlguidance B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Mrlguidance B.V. - FDA 510(k) Cleared Devices
Recent clearances: BoneMRI v1.4
1
Total
1
Cleared
0
Denied
Mrlguidance B.V. has 1 FDA 510(k) cleared medical devices. Based in Utrecht, NL.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mrlguidance B.V. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Maxis Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Mrlguidance B.V.
1 devices