Mehow Innovative, Ltd. - FDA 510(k) Cleared Devices

Mehow Innovative, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.

Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.

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

510(k) submissions have been managed by Guangzhou Osmunda Medical Device Technical Service Co., Ltd. as regulatory consultant.