K-number	K182587
Device name	Device Electrosurgical Generator ESG-150
Applicant	Olympus Winter & Ibe GmbH
Product code	GEI
Device class	Class II
Decision date	Nov 29, 2018
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Device Electrosurgical Generator ESG-150

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