LCD Monitor (MD310C, MD310G, MD210G)— 510(k) K170944

Name: FDA 510(k) clearance K170944
Creator: U.S. Food and Drug Administration
Published: 2017-05-25

Substantially Equivalent

Benq Corporation

FDA 510(k) clearance K170944 for LCD Monitor (MD310C, MD310G, MD210G), Substantially Equivalent on 2017-05-25. Applicant: Benq Corporation. Device class: 2.

Clearance details

Applicant: Benq Corporation
Product code: Code PGY
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2017-03-30
Decision date: 2017-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, TW

Download summary PDF View on FDA.gov ↗

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