K-number	K133763
Device name	SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM
Applicant	Medi-Globe Corporation
Product code	FCG
Device class	Class II
Decision date	May 15, 2014
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM

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