Tecan U.S., Ltd.

Tecan U.S., Ltd. — FDA 510(k) Submissions

Tecan U.S., Ltd. has submitted 6 FDA 510(k) premarket notifications since 1986, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Station, Pipetting And Diluting, For Clinical Use, Colorimeter, Photometer, Spectrophotometer For Clinical Use, Slide Stainer, Automated . Use the specialty filter in the sidebar to narrow results.