A & D Co., Ltd. is one of 13028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A & D Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: A&D MEDICAL UA-767F AND UA-767FAC DIGITAL BLOOD PRESSURE MONITOR, A&D MEDICAL UA-651 DIGITAL BLOOD PRESSURE MONITOR, A&D MEDICAL UB-543 DIGITAL BLOOD PRESSURE MONITOR
3
Total
3
Cleared
0
Denied
A & D Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 3 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by A & D Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A & D Co., Ltd.
3 devices