# Datrix

- Location (FDA's records): Escondido, CA
- FDA decisions: 5 (1992–2005): 5 510(k) clearances
- Product codes: MWJ (2), DSH (1), DPS (1), DQK (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 9 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Braemar, Inc.: 2 (https://510kreport.com/company/braemar)
- Reynolds Medical, Ltd.: 1 (https://510kreport.com/company/reynolds-medical)
- Quinton, Inc.: 1 (https://510kreport.com/company/quinton)

## Firms that cite its devices most
- Memtec Corp.: 2 (https://510kreport.com/company/memtec)
- Diagnostic Monitoring Software: 1 (https://510kreport.com/company/diagnostic-monitoring-software)
- Shenzhen Carewell Electronics Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-carewell-electronics)
- Diagnostic Monitoring: 1 (https://510kreport.com/company/diagnostic-monitoring)
- Intricon Datrix Corporation: 1 (https://510kreport.com/company/intricon-datrix)
- Lumedx: 1 (https://510kreport.com/company/lumedx)

## Its most-cited devices
- K052883: Cardioserver (2005), cited by 3
- K982975: Digital Ecg Holter Recorder, Model DR512 (1998), cited by 2
- K921068: Gikter Ecg Cassette Tape Recorder Model XR 300 (1992), cited by 2
- K031074: Digital Ambulatory Ecg (Holter) Recorder (2003), cited by 1
- K053083: Datrix Cardio Wifi Electrocardiograph (2005), cited by 1

## Recent decisions
- K053083: Datrix Cardio Wifi Electrocardiograph (Nov 30, 2005)
- K052883: Cardioserver (Nov 1, 2005)
- K031074: Digital Ambulatory Ecg (Holter) Recorder (Oct 15, 2003)
- K982975: Digital Ecg Holter Recorder, Model DR512 (Nov 10, 1998)
- K921068: Gikter Ecg Cassette Tape Recorder Model XR 300 (Mar 30, 1992)

Source page: https://510kreport.com/company/datrix