Medical Device Manufacturer · DE , Bendorf

Baldus Sedation GmbH & Co. KG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023

Total

Cleared

Denied

Baldus Sedation GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Bendorf, DE.

Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Baldus Sedation GmbH & Co. KG Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Baldus Sedation GmbH & Co. KG

2 devices

1-2 of 2