Columbia Scientific Development, LLC is one of 24213 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Columbia Scientific Development, LLC - FDA 510(k) Cleared Devices
Recent clearances: COLUMBIA 600 ELECTRODE, COLUMBIA 06 LEADWIRE
1
Total
1
Cleared
0
Denied
Columbia Scientific Development, LLC has 1 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Columbia Scientific Development, LLC 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 - Columbia Scientific Development, LLC
1 devices