Universal Digital Interface 2W, UDI 2W— 510(k) K143232

Name: FDA 510(k) clearance K143232
Creator: U.S. Food and Drug Administration
Published: 2015-01-30

Substantially Equivalent

Meridian Medical Systems, LLC

FDA 510(k) clearance K143232 for Universal Digital Interface 2W, UDI 2W, Substantially Equivalent on 2015-01-30. 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: 2014-11-10
Decision date: 2015-01-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Aurora, OH, US

Download summary PDF View on FDA.gov ↗

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