Zio AT® device (A100A1001)
FDA 510(k) K240029 · iRhythm Technologies, Inc.
510(k) numberK240029
Submission
- Device name
- Zio AT® device (A100A1001)
- Applicant
- iRhythm Technologies, Inc.
San Francisco, CA, US - Received
- January 4, 2024
- Decision date
- October 21, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QYX – Outpatient Cardiac Telemetry
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1025
- Specialty
- Cardiovascular
Devices are intended to continuously record and analyze electrocardiograms for automatic detection and recording of cardiac electrical activity in an outpatient setting. Detected, notifiable events are transmitted to the prescribing clinician during the monitoring period by a 24/7 attended analysis center after review by a qualified individual. Devices may allow remote access and display of…
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| K241179 | Rhythm Express Remote Cardiac Monitoring System (RX-1 mini)QYX · Traditional | VivaQuant, Inc. | 07/11/2025SE |
| K240653 | SmartCardia 7L Platform (MCT)QYX · Traditional | Smartcardia SA | 10/31/2024SE |
| K233584 | RhythmStar SystemQYX · Traditional | RhythMedix, LLC | 07/08/2024SE |
| K162956 | Nowcardio SystemQYX · Abbreviated | Contex International Technologies (Canada), Inc. | 09/22/2017SE |
| K170565 | LifeWatch Mobile Cardiac Telemetry 3 Lead LifeWatch MCT 3LQYX · Traditional | Lifewatch Services, Inc. | 08/01/2017SE |
| K163512 | Zio AT ECG Monitoring SystemQYX · Traditional | iRhythm Technologies, Inc. | 06/02/2017SE |
| K160064 | MoMe Kardia Wireless Ambulatory ECG Monitoring and Detection SystemQYX · Abbreviated | Infobionic, Inc. | 03/11/2016SE |
| K133753 | Mome ECG Continuous Detection and Arrhythmia DetectorQYX · Traditional | Infobionic, Inc. | 09/19/2014SE |
| K133701 | Nuvant MCT SystemQYX · Special | Corventis, Inc. | 02/06/2014SE |
More from Corventis, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K252859 | ZEUS Platform (FG0501US)DQK · Traditional | 05/29/2026SE |
| K243650 | Zio® monitor (DFG0001)DSH · Traditional | 08/15/2025SE |
| K240177 | Zio AT® device (A100A1001)DSI · Traditional | 10/30/2024SE |
| K222389 | ZEUS SystemDQK · Traditional | 02/15/2023SE |
| K213409 | ZEUS System (Zio Watch)DQK · Traditional | 07/19/2022SE |
| K202527 | Zio ECG Utilization Software (ZEUS) SystemDQK · Traditional | 05/21/2021SE |
| K202359 | Zio MonitorDSH · Traditional | 05/21/2021SE |
| K190593 | Zio XT ECG Monitoring System, Zio AT ECG Monitoring SystemDQK · Traditional | 08/23/2019SE |
| K181502 | Zio AT ECG Monitoring System, ZEUS SystemDQK · Traditional | 08/29/2018SE |
| K163512 | Zio AT ECG Monitoring SystemQYX · Traditional | 06/02/2017SE |
Questions and answers
When was Zio AT® device (A100A1001) cleared by the FDA?
Zio AT® device (A100A1001) (K240029) received a 510(k) decision of Substantially Equivalent on October 21, 2024, 291 days after the submission was received.
What is the product code of K240029?
The FDA product code is QYX – Outpatient Cardiac Telemetry, a Class II (moderate risk) device regulated under 21 CFR 870.1025.