Laerdal Medical A/S

Laerdal Medical A/S — FDA 510(k) Submissions

Laerdal Medical A/S has submitted 4 FDA 510(k) premarket notifications since 1999, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Valve, Non-rebreathing, Aid, Cardiopulmonary Resuscitation, Ventilator, Emergency, Manual (resuscitator), Pump, Portable, Aspiration (manual Or Powered) . Use the specialty filter in the sidebar to narrow results.