K-number	K012407
Device name	PACEART TX3 CARDIAC EVENT RECORDER
Applicant	Paceart, Inc.
Product code	DXH
Device class	Class II
Decision date	Aug 14, 2001
Decision	Substantially Equivalent
Regulation	870.2920

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View the full FDA submission: accessdata.fda.gov

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PACEART TX3 CARDIAC EVENT RECORDER

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