Class Class II

ECHELON Oval V6.2 MRI System (K221619)

K221619 2023-01-26 Traditional
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Description

ECHELON Oval V6.2 MRI System by Fujifilm Healthcare Corporation — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221619
Clearance Date2023-01-26
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000

Categories

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