APK Technology Co., Ltd.

APK Technology Co., Ltd. — FDA 510(k) Submissions

APK Technology Co., Ltd. has submitted 5 FDA 510(k) premarket notifications since 2009, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oximeter, Blood Pressure Cuff, Cable, Transducer And Electrode, Patient, (including Connector), Light, Ultraviolet, Dermatological . Use the specialty filter in the sidebar to narrow results.