MAGNETIC RESONANCE DIAGNOSTIC DEVICE— 510(k) K023929

Name: FDA 510(k) clearance K023929
Creator: U.S. Food and Drug Administration
Published: 2003-02-21

Substantially Equivalent

Advanced Imaging Research, Inc.

FDA 510(k) clearance K023929 for MAGNETIC RESONANCE DIAGNOSTIC DEVICE, Substantially Equivalent on 2003-02-21. Applicant: Advanced Imaging Research, Inc.. Device class: 2.

Clearance details

Applicant: Advanced Imaging Research, Inc.
Product code: Code MOS
Device class: Class 2
Regulation: 21 CFR 892.1000
Advisory panel: Radiology
Date received: 2002-11-25
Decision date: 2003-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

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