K-number	K922548
Device name	MEDELEC 2110 AND 2114 EEG
Applicant	Medelec Intl. Corp.
Product code	GWQ
Device class	Class II
Decision date	Nov 3, 1992
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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MEDELEC 2110 AND 2114 EEG

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