Accutome, Inc. Doing Business AS Keeler USA

Accutome, Inc. Doing Business AS Keeler USA — FDA 510(k) Submissions

Accutome, Inc. Doing Business AS Keeler USA has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Imaging, Pulsed Echo, Ultrasonic . Use the specialty filter in the sidebar to narrow results.