K-number	K202583
Device name	BioShield biopsy valve EUS - Linear
Applicant	STERIS Corporation
Product code	ODD
Device class	Class II
Decision date	Nov 6, 2020
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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BioShield biopsy valve EUS - Linear

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