Baldus Sedation GmbH & Co. KG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Kamm & Assosciates as regulatory consultant.
2 devices