Medical Device Manufacturer · US , Crofton , MD

Ueda Avancer Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

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.

Ueda Avancer Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ueda Avancer Corp.

1 devices

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