# K992908: Q-Tel Telemetry System V. 6.0 (ST)

- Pathway: 510(k) (Traditional)
- Applicant: Quinton, Inc.
- Decided: Mar 6, 2000 after 189 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K942147 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942147: Pacific Communications Model 1100, Accucore, Inc. (1995) Summary page 1.

## Indications for use
The intended use of the Q-Tel® Telemetry System v. 6.0 (ST) is the acquisition and transmission of ECG data by means of a radio-frequency transmitter worn by individual patients in a hospital or clinical setting to a central monitor where it is received, displayed, stored, and analyzed, with alarms for heart rate, arrhythmia, and ST change. The intended population are ambulatory adults where cardiac monitoring is prescribed while undergoing exercise rehabilitation.

Source page: https://510kreport.com/device/K992908
Methodology: https://510kreport.com/methodology