Dynatech Laboratories, Inc.

Dynatech Laboratories, Inc. — FDA 510(k) Submissions

Dynatech Laboratories, Inc. has submitted 44 FDA 510(k) premarket notifications since 1978, of which 44 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Colorimeter, Photometer, Spectrophotometer For Clinical Use, Device, Microtiter Diluting/dispensing, Station, Pipetting And Diluting, For Clinical Use, System, Suspension, Cell Culture, Culture Media, Multiple Biochemical Test . Use the specialty filter in the sidebar to narrow results.