Saalmann Medical GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Saalmann Medical GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Saalio
1
Total
1
Cleared
0
Denied
Saalmann Medical GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Bad Oeynhausen, DE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Saalmann Medical GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beo Medconsulting Berlin GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Saalmann Medical GmbH & Co. KG
1 devices