K-number	K162070
Device name	JOINIX CANNULAR SYSTEM
Applicant	Aju Pharm Co., Ltd.
Product code	HRX
Device class	Class II
Decision date	Mar 16, 2017
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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JOINIX CANNULAR SYSTEM

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