K-number	K020956
Device name	VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIA
Applicant	Microtek Medical, Inc.
Product code	MUI
Device class	Class II
Decision date	May 16, 2002
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIA

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