Sony Electronics, Inc. - FDA 510(k) Cleared Devices

Sony Electronics, Inc. has 8 FDA 510(k) cleared medical devices. Based in North Attleboro, US.

Historical record: 8 cleared submissions from 2009 to 2020. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Sony Electronics, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Sony Corporation, Atsugi Technology Center as regulatory consultant.