K-number	K800285
Device name	MODEL 5985 PACEMAKER PULSE GENERATOR
Applicant	Medtronic Vascular
Product code	DXY
Device class	Class III
Decision date	May 20, 1980
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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MODEL 5985 PACEMAKER PULSE GENERATOR

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