K-number	K103326
Device name	MULTIPLE BIOPSY SYSTEM
Applicant	United States Endoscopy Group, Inc.
Product code	FCK
Device class	Class II
Decision date	Apr 6, 2011
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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MULTIPLE BIOPSY SYSTEM

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