K-number	K133726
Device name	MEGA SOFT UNIVERSAL PATIENT RETURN ELECTRODE
Applicant	Megadyne Medical Products, Inc.
Product code	GEI
Device class	Class II
Decision date	Jan 24, 2014
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MEGA SOFT UNIVERSAL PATIENT RETURN ELECTRODE

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