Laerdal Medical AS

Laerdal Medical AS — FDA 510(k) Submissions

Laerdal Medical AS has submitted 5 FDA 510(k) premarket notifications since 2015, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Aid, Cardiopulmonary Resuscitation, Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms), Ventilator, Emergency, Manual (resuscitator) . Use the specialty filter in the sidebar to narrow results.