K-number	K934938
Device name	TEMPORARY SCREENING LEAD/CATHETER KIT
Applicant	Medtronic Vascular
Product code	GZB
Device class	Class II
Decision date	Jun 14, 1994
Decision	Substantially Equivalent
Regulation	882.5880

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View the full FDA submission: accessdata.fda.gov

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TEMPORARY SCREENING LEAD/CATHETER KIT

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