Medical Device Manufacturer · US , Arvada , CO

Summit Doppler Systems, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

Recent clearances: VANTAGE ABI, STN PROBE, LIFEDOP MODEL 300ABI

View 7 510(k) Devices ↓

Total

Cleared

Denied

Summit Doppler Systems, Inc. has 7 FDA 510(k) cleared medical devices. Based in Arvada, US.

Historical record: 7 cleared submissions from 2003 to 2011. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Summit Doppler Systems, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Tuv America, Inc. and Tuv Sud America, Inc..

Summit Doppler Systems, Inc. is one of 22854 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Summit Doppler Systems, Inc.

7 devices

1-7 of 7

ECHOHEART TRANSVAGINAL DOPPLER PROBE

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 15, 2026

Summit Doppler Systems, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Summit Doppler Systems, Inc.

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