Shenzhen Jamr Technology Co., Ltd.

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

Shenzhen Jamr Technology Co., Ltd. has submitted 6 FDA 510(k) premarket notifications since 2020, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Measurement, Blood-pressure, Non-invasive, Monitor, Ultrasonic, Fetal . Use the specialty filter in the sidebar to narrow results.