Packard Instrument Co., Inc.

Packard Instrument Co., Inc. — FDA 510(k) Submissions

Packard Instrument Co., Inc. has submitted 4 FDA 510(k) premarket notifications since 1988, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Microtiter Diluting/dispensing, Station, Pipetting And Diluting, For Clinical Use . Use the specialty filter in the sidebar to narrow results.