K-number	K221951
Device name	Branchor Balloon Guide Catheter
Applicant	Asahi Intecc Co., Ltd.
Product code	QJP
Device class	Class II
Decision date	Oct 11, 2022
Decision	Substantially Equivalent
Regulation	870.1250

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Source

View the full FDA submission: accessdata.fda.gov

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Branchor Balloon Guide Catheter

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