# K102206: Eli 10 Electrocardiograph Model Eli 10

- Pathway: 510(k) (Abbreviated)
- Applicant: Mortara Instrument, Inc.
- Decided: Feb 18, 2011 after 197 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K933143 (1994). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070539: Mortara Eli 10 Electrocardiograph, Mortara Instrument, Inc. (2007) Summary page 1.
- K082946: Mortara Eli 350 Electrocardiograph, Mortara Instrument, Inc. (2008) Summary page 1.

## Recalls of this device
- Mar 18, 2020 · Class II · Z-1810-2020: Impacted Welch Allyn products may not meet the Defibrillation Withstand requirements of EN/IEC 60601-2-25 Medical Electrical Equipment.

## Indications for use
The device is indicated for use to acquire, analyze, display, transmit, print, record and store electrocardiograms. 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, or mobile environment (including pre-hospital, emergency services, ambulance and patient transport), 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 EGG 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 and pediatric populations. The device is not intended to be used as a vital signs physiological monitor.

Source page: https://510kreport.com/device/K102206
Methodology: https://510kreport.com/methodology