K-number	K770328
Device name	PACEMAKER, ANTRIO-VENTRICULAR SEQ.
Applicant	American Pacemaker Corp.
Product code	DXY
Device class	Class III
Decision date	Feb 28, 1977
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PACEMAKER, ANTRIO-VENTRICULAR SEQ.

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