Puravita M, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Puravita M, LLC has 1 FDA 510(k) cleared medical devices. Based in Lindon, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Puravita M, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Iuvo Consulting, LLC as regulatory consultant.
1 devices