K-number	K183289
Device name	ClearGrasp Snare
Applicant	Finemedix Co., Ltd.
Product code	FDI
Device class	Class II
Decision date	Mar 6, 2019
Decision	Substantially Equivalent
Regulation	876.4300

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Source

View the full FDA submission: accessdata.fda.gov

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ClearGrasp Snare

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