Anumana, Inc.

Anumana, Inc. — FDA 510(k) Submissions

Anumana, Inc. has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Reduced Ejection Fraction Machine Learning-based Notification Software, Computer, Diagnostic, Programmable . Use the specialty filter in the sidebar to narrow results.