K-number	K790873
Device name	MODEL 221 PROGRAMALITH PULSE GENERATOR
Applicant	Pacesetter Systems
Product code	DXY
Device class	Class III
Decision date	Sep 20, 1979
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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MODEL 221 PROGRAMALITH PULSE GENERATOR

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