K-number	K012129
Device name	ORTHO DEVELOPMENT ORION-I EMF SYSTEM
Applicant	Ortho Development Corp.
Product code	GEI
Device class	Class II
Decision date	Aug 22, 2001
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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ORTHO DEVELOPMENT ORION-I EMF SYSTEM

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