Vivify Health, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vivify Health, Inc. has 1 FDA 510(k) cleared medical devices. Based in Plano, US.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vivify Health, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Vivify Health, Inc.
1 devices