Class Class II

RadiForce RX670; RadiForce RX670-AR (K241441)

K241441 2024-07-16 Abbreviated
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Description

RadiForce RX670; RadiForce RX670-AR by Eizo Corporation — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241441
Clearance Date2024-07-16
Clearance TypeAbbreviated
Product CodePGY
Regulation Number892.2050

Categories

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