Pronova Laboratories BV - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pronova Laboratories BV has 1 FDA 510(k) cleared medical devices. Based in Muiden, NL.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pronova Laboratories BV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pronova Laboratories BV
1 devices