K-number	K222709
Device name	Retraction, CWM-910T, APOLEX Tite
Applicant	Chungwoo Co., Ltd.
Product code	GEI
Device class	Class II
Decision date	Mar 21, 2023
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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Retraction, CWM-910T, APOLEX Tite

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