QYW — Hospital Cardiac Telemetry Class II

FDA Device Classification

Classification Details

Product Code
QYW
Device Class
Class II
Regulation Number
870.1025
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No

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 only.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K133973remote diagnostic technologiesTEMPUS PRO WITH ENHANCED FEATURESAugust 14, 2014
K934913cardiac telecomHEARTRAC ECG MONITORING SYSTEMJune 5, 1995