K-number	K051247
Device name	SONOTIP II ULTRASOUND NEEDLE SYSTEM
Applicant	Medi-Globe Corp.
Product code	FCG
Device class	Class II
Decision date	Jun 16, 2005
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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SONOTIP II ULTRASOUND NEEDLE SYSTEM

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