# Summit Doppler Systems, Inc.

- Location (FDA's records): Golden, CO
- FDA decisions: 7 (2003–2011): 7 510(k) clearances
- Product codes: JAF (2), KNG (1), HEK (1), DXN (1), ITX (1), MAA (1)
- Predicates its devices cite: 10 (5 its own); citations of its devices by later devices: 8 (5 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
- Huntleigh Healthcare, Inc.: 1 (https://510kreport.com/company/huntleigh-healthcare)
- Medasonics, Inc.: 1 (https://510kreport.com/company/medasonics)
- Atlantis Diagnostics Intl., Inc.: 1 (https://510kreport.com/company/atlantis-diagnostics-intl)
- Biomedix, Inc.: 1 (https://510kreport.com/company/biomedix)
- Imex Medical Systems, Inc.: 1 (https://510kreport.com/company/imex-medical-systems)

## Firms that cite its devices most
- Contec Medical System Co., Ltd.: 1 (https://510kreport.com/company/contec-medical-system)
- D. E. Hokanson, Inc.: 1 (https://510kreport.com/company/d-e-hokanson)
- Edan Instruments, Inc.: 1 (https://510kreport.com/company/edan-instruments)

## Its most-cited devices
- K024197: Lifedop Doppler (2003), cited by 7
- K063600: Vista Avs (2006), cited by 1

## Recent decisions
- K103693: Vantage Abi (Feb 15, 2011)
- K101816: STN Probe (Aug 19, 2010)
- K093393: Lifedop Model 300ABI (Dec 24, 2009)
- K090499: Lifedop Model, L350R (Mar 31, 2009)
- K063600: Vista Avs (Dec 19, 2006)
- K060410: Echoheart Transvaginal Doppler Probe (Apr 10, 2006)
- K024197: Lifedop Doppler (Jan 3, 2003)

Source page: https://510kreport.com/company/summit-doppler-systems