K-number	K953737
Device name	VL7600 REM PATIENT RETURN ELECTRODE
Applicant	Valleylab, Inc.
Product code	GEI
Device class	Class II
Decision date	Aug 23, 1995
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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VL7600 REM PATIENT RETURN ELECTRODE

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