Curetis GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Curetis GmbH - FDA 510(k) Cleared Devices
Recent clearances: Unyvero LRT BAL Application
2
Total
1
Cleared
1
Denied
Curetis GmbH has 1 FDA 510(k) cleared medical devices. Based in Holzgerlingen, DE.
Historical record: 1 cleared submissions from 2018 to 2019. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Curetis GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Radcliffe Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Curetis GmbH
2 devices