Renerve, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Renerve, Ltd. has 1 FDA 510(k) cleared medical devices. Based in North Melbourne, AU.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Renerve, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sloan Regulatory Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Renerve, Ltd.
1 devices