QUIX DIGITAL RADIOGRAPHIC UPGRADE— 510(k) K052661

Substantially Equivalent

Edge Medical Devices , Ltd.

FDA 510(k) clearance K052661 for QUIX DIGITAL RADIOGRAPHIC UPGRADE, Substantially Equivalent on 2006-06-07. Applicant: Edge Medical Devices , Ltd..

Clearance details

Applicant: Edge Medical Devices , Ltd.
Product code: Code MQB
Advisory panel: Radiology
Date received: 2005-09-27
Decision date: 2006-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raanana, IL

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