Provisio Medical, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Provisio Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Provisio Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Veranex, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Provisio Medical, Inc.
1 devices