Base Ten Systems, Inc.

Base Ten Systems, Inc. — FDA 510(k) Submissions

Base Ten Systems, Inc. has submitted 3 FDA 510(k) premarket notifications since 1995, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Digital Image Storage, Radiological, Calculator/data Processing Module, For Clinical Use . Use the specialty filter in the sidebar to narrow results.