Stierlen-Maquet AG

Stierlen-Maquet AG — FDA 510(k) Submissions

Stierlen-Maquet AG has submitted 10 FDA 510(k) premarket notifications since 1984, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Table, Surgical With Orthopedic Accessories, Manual, Table, Operating-room, Electrical, Table, Operating-room, Ac-powered, Table And Attachments, Operating-room . Use the specialty filter in the sidebar to narrow results.