K-number	K201650
Device name	VMCore Biopsy Needle
Applicant	Uro-1, Inc.
Product code	KNW
Device class	Class II
Decision date	Jan 15, 2021
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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VMCore Biopsy Needle

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