Duplex International Trading Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Duplex International Trading Limited has 1 FDA 510(k) cleared medical devices. Based in Hong Kong, CN.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Duplex International Trading Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai CV Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Duplex International Trading Limited
1 devices