UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W— 510(k) K111305

Name: FDA 510(k) clearance K111305
Creator: U.S. Food and Drug Administration
Published: 2012-01-31

Substantially Equivalent

Meridian Medical Systems, LLC

FDA 510(k) clearance K111305 for UNIVERSAL DIGITAL INTERFACE WIRELESS - UDI 1417W, Substantially Equivalent on 2012-01-31. Applicant: Meridian Medical Systems, LLC. Device class: 2.

Clearance details

Applicant: Meridian Medical Systems, LLC
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2011-05-09
Decision date: 2012-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aurora, OH, US

Download summary PDF View on FDA.gov ↗

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