K-number	K120781
Device name	CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH
Applicant	Fuji Systems Corp.
Product code	DQY
Device class	Class II
Decision date	Aug 9, 2012
Decision	Substantially Equivalent
Regulation	870.1250

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View the full FDA submission: accessdata.fda.gov

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CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH

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