UNIVERSAL DIGITAL INTERFACE 2, UDI 2— 510(k) K140251

Name: FDA 510(k) clearance K140251
Creator: U.S. Food and Drug Administration
Published: 2014-10-22

Substantially Equivalent

Meridian Medical Systems, LLC

FDA 510(k) clearance K140251 for UNIVERSAL DIGITAL INTERFACE 2, UDI 2, Substantially Equivalent on 2014-10-22. 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: 2014-01-31
Decision date: 2014-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aurora, OH, US

Download summary PDF View on FDA.gov ↗

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