K-number	K112828
Device name	REVIVE INTERMEDIATE CATHETER (REVIVE IC)
Applicant	Codman & Shurtleff, Inc.
Product code	DQY
Device class	Class II
Decision date	Oct 25, 2011
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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REVIVE INTERMEDIATE CATHETER (REVIVE IC)

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