K-number	K171454
Device name	Interject Injection Therapy Needle Catheter
Applicant	Boston Scientific Corporation
Product code	FBK
Device class	Class II
Decision date	Jul 7, 2017
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Interject Injection Therapy Needle Catheter

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