K-number	K192128
Device name	Sutter Arrowtip Monopolar Electrodes
Applicant	Sutter Medizintechnik GmbH
Product code	GEI
Device class	Class II
Decision date	Oct 4, 2019
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Sutter Arrowtip Monopolar Electrodes

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