DDRVERSA MOTION— 510(k) K123005

Substantially Equivalent

Swissray Medical AG

FDA 510(k) clearance K123005 for DDRVERSA MOTION, Substantially Equivalent on 2012-12-07. Applicant: Swissray Medical AG. Device class: 2.

Clearance details

Applicant: Swissray Medical AG
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2012-09-27
Decision date: 2012-12-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Naples, FL, US

Download summary PDF View on FDA.gov ↗

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