Duomed, Inc. is one of 25741 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Duomed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DUOMED, SERIES 500, (MODELS ID 500, FL 500)
1
Total
1
Cleared
0
Denied
Duomed, Inc. has 1 FDA 510(k) cleared medical devices. Based in West Palm Beach, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Duomed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Duomed, Inc.
1 devices