ClearanceBrief
Company ยท US

Corventis, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2014. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QYXOutpatient Cardiac Telemetry4
DSIDetector And Alarm, Arrhythmia2
MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 6, 2014K133701NUVANT MCT SYSTEM
Corventis, Inc.
QYX
Mar 7, 2012K113372NUVANT, MOBILC CARDIAC TELEMETRY
Corventis, Inc.
QYX
Jan 4, 2012K113187AVIVO MOBILE PATIENT MANAGEMENT
Corventis, Inc.
MHX
Aug 24, 2011K111917NUVANT, MOBILE CARDIAC TELEMETRY
Corventis, Inc.
QYX
Aug 27, 2009K091971AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM
Corventis, Inc.
DSI
Jun 19, 2009K090696NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM
Corventis, Inc.
QYX
Feb 3, 2009K083287AVIVO MOBILE PATIENT MANAGEMENT SYSTEM
Corventis, Inc.
DSI

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes