K-number	K910237
Device name	MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR
Applicant	Medtronic Vascular
Product code	DTE
Device class	Class II
Decision date	Feb 25, 1991
Decision	Substantially Equivalent
Regulation	870.3600

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View the full FDA submission: accessdata.fda.gov

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MODIFIED MODEL 5330 AV DEMAND PULSE GENERATOR

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