Nuvoair AB is one of 54 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Nuvoair AB - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Nuvoair AB has 2 FDA 510(k) cleared medical devices. Based in Stockholm, SE.
Latest FDA clearance: Jan 2024. Active since 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Nuvoair AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Nuvoair AB
2 devices