K-number	K893633
Device name	MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE
Applicant	Medtronic Vascular
Product code	DTE
Device class	Class II
Decision date	Jun 20, 1989
Decision	Substantially Equivalent
Regulation	870.3600

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View the full FDA submission: accessdata.fda.gov

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MODEL 5330 EXTERNAL A-V SEQUENTIAL DEMAND PULSE

Everything you need for a 510(k) submission. Nothing you don't.