Seiratherm GmbH is one of 494 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Seiratherm GmbH has 1 FDA 510(k) cleared medical devices. Based in 91074 Herzogenaurach, DE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Seiratherm GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philosopher'S River, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Seiratherm GmbH
1 devices