Medical Device Manufacturer · JP , Komaki

Santec Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015

Total

Cleared

Denied

Santec Corporation has 2 FDA 510(k) cleared medical devices. Based in Komaki, JP.

Historical record: 2 cleared submissions from 2015 to 2019. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Santec Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Santec Corporation

2 devices

1-2 of 2