K-number	K233982
Device name	CEREGLIDE 92 Catheter System
Applicant	Cerenovus, Inc.
Product code	QJP
Device class	Class II
Decision date	May 9, 2024
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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CEREGLIDE 92 Catheter System

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