Ueda Avancer Corp. is one of 13130 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ueda Avancer Corp. - FDA 510(k) Cleared Devices
Recent clearances: UEDA UDEX SUPER BP-2000 AUTOMATIC BLOOD PRESSURE RECORDING DEVICE
1
Total
1
Cleared
0
Denied
Ueda Avancer Corp. has 1 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ueda Avancer Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ueda Avancer Corp.
1 devices