K-number	K091992
Device name	EIDOSMED, MODEL EDG4.0
Applicant	Eidosmed, LLC
Product code	OOL
Device class	Class II
Decision date	Dec 9, 2009
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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EIDOSMED, MODEL EDG4.0

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