K-number	K200298
Device name	ABI Instrument, Creo Electrosurgical System
Applicant	Creo Medical, Ltd.
Product code	NEY
Device class	Class II
Decision date	Jan 5, 2021
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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ABI Instrument, Creo Electrosurgical System

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