FDA 510(k) Applications Submitted by CORVENTIS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K133701 |
12/03/2013 |
NUVANT MCT SYSTEM |
CORVENTIS, INC. |
| K083287 |
11/07/2008 |
AVIVO MOBILE PATIENT MANAGEMENT SYSTEM |
CORVENTIS, INC. |
| K113187 |
10/31/2011 |
AVIVO MOBILE PATIENT MANAGEMENT |
CORVENTIS, INC. |
| K113372 |
11/16/2011 |
NUVANT, MOBILC CARDIAC TELEMETRY |
CORVENTIS, INC. |
| K090696 |
03/16/2009 |
NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEM |
CORVENTIS, INC. |
| K091971 |
07/01/2009 |
AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEM |
CORVENTIS, INC. |
| K111917 |
07/06/2011 |
NUVANT, MOBILE CARDIAC TELEMETRY |
CORVENTIS, INC. |
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