Medical Device Manufacturer · US , Hillsborough , NC

Tecan U.S., Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1986

Total

Cleared

Denied

Tecan U.S., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Hillsborough, US.

Historical record: 6 cleared submissions from 1986 to 1994. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Tecan U.S., Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tecan U.S., Ltd.

6 devices

1-6 of 6