K-number	K113607
Device name	BIOPSY DIGIT S BIOPSY SL
Applicant	Giotto USA, LLC
Product code	IZH
Device class	Class II
Decision date	Aug 10, 2012
Decision	Substantially Equivalent
Regulation	892.1710

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View the full FDA submission: accessdata.fda.gov

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BIOPSY DIGIT S BIOPSY SL

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