Class Class II

ECHELON Synergy MRI System (K241429)

K241429 2024-08-13 Traditional
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK241429
Clearance Date2024-08-13
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000

Categories

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