Medical Device Manufacturer · SE , Stockholm

Nuvoair AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2020

Total

Cleared

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.

FDA 510(k) cleared devices by Nuvoair AB

2 devices

1-2 of 2