Panthera AB - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Panthera AB has 1 FDA 510(k) cleared medical devices. Based in Stockholm, SE.
Last cleared in 2023. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Panthera AB 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 - Panthera AB
1 devices