Bracco Injeneering is one of 139 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Bracco Injeneering - FDA 510(k) Cleared Devices
Recent clearances: CT Expres 3D Contrast Media Delivery System, Bottle Spike Type B, Day Set III HP, Patient Set
1
Total
1
Cleared
0
Denied
Bracco Injeneering has 1 FDA 510(k) cleared medical devices. Based in Lausanne, CH.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bracco Injeneering Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Icon Clinical Research, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Bracco Injeneering
1 devices