K-number	K791955
Device name	UNIFOCAL 1 UNIPOLAR DEMAND R WAVE
Applicant	American Pacemaker Corp.
Product code	DXY
Device class	Class III
Decision date	Nov 27, 1979
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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UNIFOCAL 1 UNIPOLAR DEMAND R WAVE

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