Vivaquant, Inc.

Vivaquant, Inc. — FDA 510(k) Submissions

Vivaquant, Inc. has submitted 3 FDA 510(k) premarket notifications since 2019, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Transmitters And Receivers, Electrocardiograph, Telephone, Electrocardiograph, Ambulatory, With Analysis Algorithm, Outpatient Cardiac Telemetry . Use the specialty filter in the sidebar to narrow results.