Civco is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Civco - FDA 510(k) Cleared Devices
Recent clearances: ETRAX NEEDLE SYSTEM, ETRAX VARIABLE ANGLE NEEDLE GUIDANCE SYSTEM, VIRTUTRAX UNIVERSAL TRACKER, FIDUCIAL MARKERS
2
Total
2
Cleared
0
Denied
Civco has 2 FDA 510(k) cleared medical devices. Based in Orange City, US.
Historical record: 2 cleared submissions from 2007 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Civco Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Civco
2 devices