K-number	K014137
Device name	MODIFICATION TO EBI OMEGA 21 SYSTEM
Applicant	Ebi, L.P.
Product code	MNH
Device class	Class II
Decision date	Jan 16, 2002
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO EBI OMEGA 21 SYSTEM

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