K-number	K790141
Device name	PULSE GENERATOR, R WAVE DEMAND
Applicant	Pacesetter Systems
Product code	DXY
Device class	Class III
Decision date	Aug 10, 1979
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PULSE GENERATOR, R WAVE DEMAND

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