Otto Bock Pur Life Science GmbH

Otto Bock Pur Life Science GmbH — FDA 510(k) Submissions

Otto Bock Pur Life Science GmbH has submitted 1 FDA 510(k) premarket notifications since 2009, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spatula, Cervical, Cytological . Use the specialty filter in the sidebar to narrow results.