Class Class II

BoneMRI v1.6 (K230197)

K230197 2023-02-22 Special
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Description

BoneMRI v1.6 by Mriguidance B.V. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230197
Clearance Date2023-02-22
Clearance TypeSpecial
Product CodeQIH
Regulation Number892.2050

Categories

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