K-number	K201244
Device name	Concorde Models Concorde US and Concorde ST Soft Tissue Biopsy Devices
Applicant	Transmed7, LLC
Product code	KNW
Device class	Class II
Decision date	Aug 7, 2020
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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Concorde Models Concorde US and Concorde ST Soft Tissue Biopsy Devices

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