Vyvo Technology Corp.(Vt) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vyvo Technology Corp.(Vt) has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Latest FDA clearance: Mar 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vyvo Technology Corp.(Vt) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Global Medical Technology Services Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Vyvo Technology Corp.(Vt)
1 devices