K-number	K860988
Device name	RMI CAROTID BY-PASS SHUNT
Applicant	Research Medical, Inc.
Product code	DWF
Device class	Class II
Decision date	May 21, 1986
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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RMI CAROTID BY-PASS SHUNT

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