Medical Device Manufacturer · US , Great Neck , NY

Sakura Seiki Co., Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012

Total

Cleared

Denied

Sakura Seiki Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 3 cleared submissions from 2012 to 2014. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Sakura Seiki Co., Ltd. Filter by specialty or product code using the sidebar.

Sakura Seiki Co., Ltd. is one of 5140 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Sakura Seiki Co., Ltd. — FDA 510(k) Products and Clearance History

3 devices

1-3 of 3