# K152701: Matrix Mini ECG Monitor

- Pathway: 510(k) (Abbreviated)
- Applicant: Global Instrumentation, LLC
- Decided: Apr 22, 2016 after 214 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: 5 generations back to K925411 (1993). 12 ancestors in all.
3 later devices descend from it; 1 cites it directly.
1 of 16 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984033: Atlas Monitor, Welch Allyn, Inc. (1999) Summary page 4.
- K120774: Acuity Central Monitoring Station or Acuity Central Monitoring System, Mobile Acuity LT, Mobile Acuity, Mobile LT, Welch Allyn, Inc. (2012) Summary page 4.

## Most influential descendants
- K171621: Welch Allyn Connex Vital Signs Monitor, Welch Allyn Connex Integrated Wall System, 901060 Vital Signs Monitor (2017), 2 descendants of its own
- K212473: Welch Allyn Connex Central Station (2022), 0 descendants of its own
- K201635: MouthLab Vital Signs Monitoring System (2021), 0 descendants of its own

## Indications for use
The Matrix Mini ECG Monitor is intended for continuous measurement of heart rate, respiration rate and detection of cardiac standstill (asystole), ventricular tachycardia and ventricular fibrillation in general medical and surgical floors, general hospital and alternate professional healthcare environments. The system is indicated for use in pediatric and adult patients.

Source page: https://510kreport.com/device/K152701
Methodology: https://510kreport.com/methodology