K-number	K885267
Device name	VS-1 MODEL NUMBER 251K PULSE GENERATOR
Applicant	Pacesetter Systems
Product code	DXY
Device class	Class III
Decision date	Mar 28, 1989
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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VS-1 MODEL NUMBER 251K PULSE GENERATOR

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