Medical Device Manufacturer · US , Wallingford , CT

Aloka Co. Ltd USA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Total

Cleared

Denied

Aloka Co. Ltd USA has 2 FDA 510(k) cleared medical devices. Based in Wallingford, US.

Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Aloka Co. Ltd USA

2 devices

1-2 of 2