K-number	K111917
Device name	NUVANT, MOBILE CARDIAC TELEMETRY
Applicant	Corventis, Inc.
Product code	QYX
Device class	Class II
Decision date	Aug 24, 2011
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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NUVANT, MOBILE CARDIAC TELEMETRY

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