K-number	K193380
Device name	CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set
Applicant	Codman & Shurtleff, Inc.
Product code	NRY
Device class	Class II
Decision date	Jul 20, 2020
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set

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