Eresearchtechnology GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Eresearchtechnology GmbH - FDA 510(k) Cleared Devices
Recent clearances: SpiroSphere, SpiroSphereECG, CardioSphere, MasterScope, MasterScope CT, MasterScope ECG, MasterScope WSSU, SpiroSphere
3
Total
3
Cleared
0
Denied
Eresearchtechnology GmbH has 3 FDA 510(k) cleared medical devices. Based in Estenfeld, DE.
Latest FDA clearance: May 2024. Active since 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Eresearchtechnology GmbH Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Sud America, Inc. and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Eresearchtechnology GmbH
3 devices