K-number	K062041
Device name	MODEL 3875 1 X 8 SC TEST STIMULATION LEAD
Applicant	Medtronic, Inc.
Product code	GZB
Device class	Class II
Decision date	Aug 16, 2006
Decision	Substantially Equivalent
Regulation	882.5880

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View the full FDA submission: accessdata.fda.gov

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MODEL 3875 1 X 8 SC TEST STIMULATION LEAD

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