K-number	K140051
Device name	KJ EXTERNAL IMPLANT SYSTEM
Applicant	Kj Meditech Co., Ltd.
Product code	DZE
Device class	Class II
Decision date	Oct 30, 2014
Decision	Substantially Equivalent
Regulation	872.3640

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Source

View the full FDA submission: accessdata.fda.gov

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KJ EXTERNAL IMPLANT SYSTEM

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