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