K-number	K190909
Device name	ArtiSential Bipolar Fenestrated Forceps
Applicant	Livsmed, Inc.
Product code	GEI
Device class	Class II
Decision date	Feb 13, 2020
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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ArtiSential Bipolar Fenestrated Forceps

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