Avivo Mobile Patient Management System
FDA 510(k) K083287 · Corventis, Inc.
510(k) numberK083287
Submission
- Device name
- Avivo Mobile Patient Management System
- Applicant
- Corventis, Inc.
San Jose, CA, US - Received
- November 7, 2008
- Decision date
- February 3, 2009
- Decision
- Substantially Equivalent (SESE)
- Type
- Abbreviated 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DSI – Detector And Alarm, Arrhythmia
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1025
- Specialty
- Cardiovascular
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| K243349 | BodyGuardian Remote Monitoring System (BGRMS v3.0)DSI · Traditional | Boston Scientific Cardiac Diagnostic… | 01/23/2026SE |
| K250356 | MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)DSI · Traditional | Infobionic, Inc. | 07/29/2025SE |
| K240177 | Zio AT® device (A100A1001)DSI · Traditional | iRhythm Technologies, Inc. | 10/30/2024SE |
| K230265 | MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemDSI · Abbreviated | Infobionic, Inc. | 10/06/2023SE |
| K231276 | SmartCardia 7L PlatformDSI · Traditional | Smartcardia SA | 08/30/2023SE |
| K193104 | Unified Arrhythmia Diagnostic System PocketECG IVDSI · Special | Medicalgorithmics S.A. | 04/09/2020SE |
| K192732 | BodyGuardian Remote Monitoring SystemDSI · Traditional | Preventice Technologies, Inc. | 03/26/2020SE |
| K190574 | Patient Assistant Model PA97000DSI · Traditional | Medtronic, Inc. | 09/24/2019SE |
| K182532 | Liba3 SystemDSI · Traditional | National Cardiac, Inc. | 05/15/2019SE |
| K181658 | MobileECG 2 BTDSI · Traditional | Memtec Corporation | 03/26/2019SE |
More from Memtec Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K133701 | Nuvant MCT SystemQYX · Special | 02/06/2014SE |
| K113372 | Nuvant, Mobilc Cardiac TelemetryQYX · Special | 03/07/2012SE |
| K113187 | Avivo Mobile Patient ManagementMHX · Abbreviated | 01/04/2012SE |
| K111917 | Nuvant, Mobile Cardiac TelemetryQYX · Abbreviated | 08/24/2011SE |
| K091971 | Avivo Mobile Patient Management System, Nuvant Mobile Cardiac Telemetry (MCT) SystemDSI · Special | 08/27/2009SE |
| K090696 | Nuvant Cardiac Event Monitoring System; Nuvant Mobile Cardiac Telemetry SystemQYX · Special | 06/19/2009SE |
Questions and answers
When was Avivo Mobile Patient Management System cleared by the FDA?
Avivo Mobile Patient Management System (K083287) received a 510(k) decision of Substantially Equivalent on February 3, 2009, 88 days after the submission was received.
What is the product code of K083287?
The FDA product code is DSI – Detector And Alarm, Arrhythmia, a Class II (moderate risk) device regulated under 21 CFR 870.1025.