K-number	K780001
Device name	EPIDURAL LEAD - MODEL 3481
Applicant	Medtronic Vascular
Product code	GZB
Device class	Class II
Decision date	Jan 17, 1978
Decision	Substantially Equivalent
Regulation	882.5880

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View the full FDA submission: accessdata.fda.gov

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EPIDURAL LEAD - MODEL 3481

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