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Corventis, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K133701NUVANT MCT SYSTEMFebruary 6, 2014
K113372NUVANT, MOBILC CARDIAC TELEMETRYMarch 7, 2012
K113187AVIVO MOBILE PATIENT MANAGEMENTJanuary 4, 2012
K111917NUVANT, MOBILE CARDIAC TELEMETRYAugust 24, 2011
K091971AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEMAugust 27, 2009
K090696NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEMJune 19, 2009
K083287AVIVO MOBILE PATIENT MANAGEMENT SYSTEMFebruary 3, 2009