DeepHealth, Inc.

DeepHealth, Inc. — FDA 510(k) Submissions

DeepHealth, Inc. has submitted 8 FDA 510(k) premarket notifications since 2021, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Radiological Computer Assisted Detection/diagnosis Software For Lesions Suspicious For Cancer, Automated Radiological Image Processing Software, Radiological Computer-assisted Prioritization Software For Lesions, System, Image Processing, Radiological . Use the specialty filter in the sidebar to narrow results.