Mediana Co., Ltd. - FDA 510(k) Cleared Devices

Mediana Co., Ltd. has 10 FDA 510(k) cleared medical devices. Based in Flintville, US.

Historical record: 10 cleared submissions from 2005 to 2020. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Mediana Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by International Regulatory Consultants as regulatory consultant.