K-number	K850605
Device name	RADI-BIOPSY DEVICE
Applicant	Radiplast AB
Product code	KNW
Device class	Class II
Decision date	Aug 9, 1985
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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RADI-BIOPSY DEVICE

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