Senzime AB is one of 54 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Senzime AB - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Senzime AB has 2 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Last cleared in 2022. Active since 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Senzime AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Obelix Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Senzime AB
2 devices