K-number	K891383
Device name	MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM
Applicant	Oxford Medilog, Inc.
Product code	OLZ
Device class	Class II
Decision date	Jun 1, 1989
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM

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