# Deltex Medical Limited

- Location (FDA's records): Chichester, West Sussex, GB
- FDA decisions: 9 (1995–2018): 9 510(k) clearances
- Names in FDA's records: Deltex Medical Limited (6); Deltex Medical (3)
- Product codes: DPW (6), DPT (3)
- Predicates its devices cite: 14 (12 its own); citations of its devices by later devices: 13 (12 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vasocom, Inc.: 1 (https://510kreport.com/company/vasocom)
- Sometec, Inc.: 1 (https://510kreport.com/company/sometec)

## Firms that cite its devices most
- Sometec, Inc.: 1 (https://510kreport.com/company/sometec)

## Its most-cited devices
- K111542: Deltex Medical Cardioq Edm (2011), cited by 3
- K031706: Cardioq, Model 9051-7005 (2003), cited by 3
- K132139: Deltex Medical Cardioq-Edm+ (2013), cited by 2
- K951369: EDM (1995), cited by 2
- K052989: DP240 240 Hour Doppler Probe (2006), cited by 2
- K073593: I2S Doppler Probe ( 6 Hour), I2S Doppler Probe (24 Hour), I2C Doppler Probe (72 Hour), Models 9090-7015, 9090-7016 (2009), cited by 1

## Recent decisions
- K172457: Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM (Jun 28, 2018)
- K150347: Deltex Medical CardioQ-EDM, Deltex Medical CardioQ-EDM+ (Jul 24, 2015)
- K142932: Deltex Medical KDP72 Doppler Probe (Jan 22, 2015)
- K132139: Deltex Medical Cardioq-Edm+ (Oct 10, 2013)
- K111542: Deltex Medical Cardioq Edm (Oct 20, 2011)
- K073593: I2S Doppler Probe ( 6 Hour), I2S Doppler Probe (24 Hour), I2C Doppler Probe (72 Hour), Models 9090-7015, 9090-7016 (Jan 29, 2009)
- K052989: DP240 240 Hour Doppler Probe (Mar 8, 2006)
- K031706: Cardioq, Model 9051-7005 (Aug 6, 2003)

Source page: https://510kreport.com/company/deltex-medical