K-number	K201771
Device name	Single Use Rotatable and Repositionable Hemoclip
Applicant	Anrei Medical (Hangzhou) Co., Ltd.
Product code	PKL
Device class	Class II
Decision date	Oct 19, 2020
Decision	Substantially Equivalent
Regulation	876.4400

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View the full FDA submission: accessdata.fda.gov

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Single Use Rotatable and Repositionable Hemoclip

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