RadiForce RX560, RX560-AR— 510(k) K172738

Substantially Equivalent

Eizo Corporation

FDA 510(k) clearance K172738 for RadiForce RX560, RX560-AR, Substantially Equivalent on 2017-11-08. Applicant: Eizo Corporation. Device class: 2.

Clearance details

Applicant: Eizo Corporation
Product code: Code PGY
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2017-09-12
Decision date: 2017-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hakusan, JP

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.