Nexus DR Digital X-ray Imaging System (with PaxScan 4343RC and PaxScan 4343Rv3)— 510(k) K172951

Name: FDA 510(k) clearance K172951
Creator: U.S. Food and Drug Administration
Published: 2017-10-24

Substantially Equivalent

Varex Imaging Corporation

FDA 510(k) clearance K172951 for Nexus DR Digital X-ray Imaging System (with PaxScan 4343RC and PaxScan 4343Rv3), Substantially Equivalent on 2017-10-24. 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: 2017-09-26
Decision date: 2017-10-24
Decision: Substantially Equivalent
Clearance type: Special
Location: Liverpool, NY, US

Download summary PDF View on FDA.gov ↗

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