K-number	K760669
Device name	PACEMAKERS, VITATRON'S
Applicant	Vitatron Medical BV
Product code	DXY
Device class	Class III
Decision date	Nov 12, 1976
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PACEMAKERS, VITATRON'S

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