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Corventis, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K113372	NUVANT, MOBILC CARDIAC TELEMETRY	QYX	2012-03-07	View
510(k)	K113187	AVIVO MOBILE PATIENT MANAGEMENT	MHX	2012-01-04	View
510(k)	K111917	NUVANT, MOBILE CARDIAC TELEMETRY	QYX	2011-08-24	View
510(k)	K091971	AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM	DSI	2009-08-27	View
510(k)	K090696	NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM	QYX	2009-06-19	View
510(k)	K083287	AVIVO MOBILE PATIENT MANAGEMENT SYSTEM	DSI	2009-02-03	View

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