K-number	K780741
Device name	GENERATOR, PULSE, DEMAND, MODEL 5996
Applicant	Medtronic Vascular
Product code	DXY
Device class	Class III
Decision date	Jul 28, 1978
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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GENERATOR, PULSE, DEMAND, MODEL 5996

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