Heartsine Technologies, Inc.

Heartsine Technologies, Inc. — FDA 510(k) Submissions

Heartsine Technologies, Inc. has submitted 6 FDA 510(k) premarket notifications since 2003, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Automated External Defibrillators (non-wearable) . Use the specialty filter in the sidebar to narrow results.