QYW
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Hospital Cardiac Telemetry
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1025
- Medical specialty
- Cardiovascular
- Flags
- Life-sustaining
- FDA definition
- Devices are intended to continuously record, display, and/or analyze electrocardiograms of patients in in a healthcare facility for detecting conditions that may require prompt intervention. They may include automatic detection and recording of cardiac electrical activity, automated detection of life-threatening arrhythmias or other relevant conditions, and/or alarm generation. Devices may allow remote access and display of electrocardiograms acquired. Devices are intended for patients who require continuous monitoring in hospitals or healthcare facilities, with onsite medical review by qualified personnel at the central monitoring/analysis station followed by immediate notification of onsite qualified medical responders. Devices may be used for patients at elevated risk of serious cardiovascular events that would require prompt intervention. Devices are intended for prescription use onl
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| TEMPUS PRO WITH ENHANCED FEATURES (K133973) | Remote Diagnostic Technologies , Ltd. | 2014-08-14 |
| HEARTRAC ECG MONITORING SYSTEM (K934913) | Cardiac Telecom Corp. | 1995-06-05 |
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Every clearance here is in the API, with alerts when new ones post.