K-number	K221930
Device name	CEREGLIDE 71 Intermediate Catheter
Applicant	Cerenovus, Inc.
Product code	QJP
Device class	Class II
Decision date	Mar 9, 2023
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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CEREGLIDE 71 Intermediate Catheter

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