Medical Device Manufacturer · US , San Jose , CA

Goldway Us, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Total

Cleared

Denied

Goldway Us, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Jose, US.

Historical record: 4 cleared submissions from 2003 to 2012. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Goldway Us, Inc. Filter by specialty or product code using the sidebar.

Goldway Us, Inc. is one of 5407 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Goldway Us, Inc. — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4