K-number	K130282
Device name	REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT
Applicant	Remington Medical, Inc.
Product code	KNW
Device class	Class II
Decision date	May 13, 2013
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT

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