K-number	K850652
Device name	PACESETTER SYSTEMS, ENDOCARDIAL FIRM LEAD
Applicant	Pacesetter Systems
Product code	DTD
Device class	Class II
Decision date	Apr 10, 1985
Decision	Substantially Equivalent
Regulation	870.3620

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View the full FDA submission: accessdata.fda.gov

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PACESETTER SYSTEMS, ENDOCARDIAL FIRM LEAD

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