Civatech Oncology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Civatech Oncology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CivaDerm
3
Total
3
Cleared
0
Denied
Civatech Oncology, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mebane, US.
Historical record: 3 cleared submissions from 2008 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Civatech Oncology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by TAMM Net, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Civatech Oncology, Inc.
3 devices