K-number	K022638
Device name	NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT
Applicant	Neurorecovery, Inc.
Product code	GWM
Device class	Class II
Decision date	Oct 31, 2002
Decision	Substantially Equivalent
Regulation	882.1620

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View the full FDA submission: accessdata.fda.gov

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NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT

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