Baldus Sedation GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Baldus Sedation GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: FlowStar Analog Mixer Flowmeter, FlowStar Touch Digital Mixer Flowmeter
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.
FDA 510(k) Regulatory Record - Baldus Sedation GmbH & Co. KG
2 devices