Pneumeric, Inc.

Pneumeric, Inc. — FDA 510(k) Submissions

Pneumeric, Inc. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Aspiration And Injection, Disposable . Use the specialty filter in the sidebar to narrow results.