Diasia Biomedical Technology Co., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Diasia Biomedical Technology Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Diasia Biomedical Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Joyantech Consulting Co., Ltd. as regulatory consultant.
1 devices