K-number	K090611
Device name	REVOLUTION FULL CORE BIOPSY
Applicant	Inrad
Product code	KNW
Device class	Class II
Decision date	Jun 4, 2009
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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REVOLUTION FULL CORE BIOPSY

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