DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9— 510(k) K073056

Name: FDA 510(k) clearance K073056
Creator: U.S. Food and Drug Administration
Published: 2007-11-13

Substantially Equivalent

Vieworks Co., Ltd.

FDA 510(k) clearance K073056 for DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9, Substantially Equivalent on 2007-11-13. Applicant: Vieworks Co., Ltd.. Device class: 2.

Clearance details

Applicant: Vieworks Co., Ltd.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2007-10-30
Decision date: 2007-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gyeonggi-Do, KR

Download summary PDF View on FDA.gov ↗

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