VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIA— 510(k) K020956

Name: FDA 510(k) clearance K020956
Creator: U.S. Food and Drug Administration
Published: 2002-05-16

Substantially Equivalent

Microtek Medical, Inc.

FDA 510(k) clearance K020956 for VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIA, Substantially Equivalent on 2002-05-16. Applicant: Microtek Medical, Inc.. Device class: 2.

Clearance details

Applicant: Microtek Medical, Inc.
Product code: Code MUI
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 2002-03-25
Decision date: 2002-05-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, MS, US

Download summary PDF View on FDA.gov ↗

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