# K070539: Mortara Eli 10 Electrocardiograph

- Pathway: 510(k) (Special)
- Applicant: Mortara Instrument, Inc.
- Decided: Mar 15, 2007 after 17 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- 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 K851702 (1985). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K851702: Mortara Instrument Model EL-1, Mortara Instrument, Inc. (1985) Summary page 1.

## Most influential descendants
- K102206: Eli 10 Electrocardiograph Model Eli 10 (2011), 0 descendants of its own

## Indications for use
The device is indicated for use to acquire, analyze, display and print electrocardiograms. (printing function available only through an external, optional printer) The device is indicated for use to provide interpretation of the data for consideration by a physician. The device is indicated for use in a clinical setting, by a physician or by trained personnel who are acting on the orders of a licensed physician. It is not intended as a sole means of diagnosis. The interpretations of ECG offered by the device are only significant when used in conjunction with a physician over-read as well as consideration of all other relevant patient data. The device is indicated for use on adult populations. The device is indicated for use on pediatric populations for acquisition, display, and printing of multi-channel ECGs. The device is not intended to be used as a vital signs physiological monitor.

Source page: https://510kreport.com/device/K070539
Methodology: https://510kreport.com/methodology