# K961014: Quinton Model Q710 Exercise and Resting Electrocardiograph

- Pathway: 510(k) (Traditional)
- Applicant: Quinton, Inc.
- Decided: Jul 31, 1996 after 140 days
- Product code: LOS
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Hewlett Packard Pagewriter XLi M1700A: named in the summary without a submission number

## Indications for use
The intended uses of the Quinton Model Q710 Exercise and Resting Electrocardiograph are acquisition, digitization, display, and recording of conventional diagnostic 12 simultaneous lead ECG waveforms and ECG data. As an option, the Model Q710 has a resting ECG analysis program which makes measurements and provides interpretation of the ECG waveform for both adult and pediatric populations. This analysis program is offered to the physician on an advisory basis only and the physician is asked to overread and validate (or change) the ECG interpretation.

Source page: https://510kreport.com/device/K961014
Methodology: https://510kreport.com/methodology