Nexus DR Digital X-ray Imaging System— 510(k) K171138

Name: FDA 510(k) clearance K171138
Creator: U.S. Food and Drug Administration
Published: 2017-05-17

Substantially Equivalent

Varex Imaging Corporation

FDA 510(k) clearance K171138 for Nexus DR Digital X-ray Imaging System, Substantially Equivalent on 2017-05-17. Applicant: Varex Imaging Corporation. Device class: 2.

Clearance details

Applicant: Varex Imaging Corporation
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2017-04-18
Decision date: 2017-05-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Liverpool, NY, US

Download summary PDF View on FDA.gov ↗

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