K-number	K191322
Device name	E-EEGX, N-EEGX
Applicant	GE Healthcare Finland Oy
Product code	OLT
Device class	Class II
Decision date	Jan 22, 2020
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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E-EEGX, N-EEGX

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