Medical Device Manufacturer · US , West Palm Beach , FL

Duomed, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Recent clearances: DUOMED, SERIES 500, (MODELS ID 500, FL 500)

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Duomed, Inc. Neurology ✕

1 devices

1-1 of 1

Cleared Mar 18, 2003

DUOMED, SERIES 500, (MODELS ID 500, FL 500)

Neurology · 63d