A&D Medical Div. is one of 13130 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A&D Medical Div. - FDA 510(k) Cleared Devices
Recent clearances: A&D MEDICAL TM-2430 AND TM-2431 AMBULATORY BLOOD PRESSURE
1
Total
1
Cleared
0
Denied
A&D Medical Div. has 1 FDA 510(k) cleared medical devices. Based in Milpitas, US.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by A&D Medical Div. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - A&D Medical Div.
1 devices