K-number	K233988
Device name	Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set
Applicant	Cerenovus, Inc.
Product code	NRY
Device class	Class II
Decision date	Jan 17, 2024
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set

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