Dynatech Corp.

Dynatech Corp. — FDA 510(k) Submissions

Dynatech Corp. has submitted 27 FDA 510(k) premarket notifications since 1979, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, General Purpose, Microbiology, Diagnostic, Device, Microtiter Diluting/dispensing, Colorimeter, Photometer, Spectrophotometer For Clinical Use, Station, Pipetting And Diluting, For Clinical Use, Dish, Tissue Culture . Use the specialty filter in the sidebar to narrow results.