Cadwell is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cadwell - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cadwell has 2 FDA 510(k) cleared medical devices. Based in Kennewick, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cadwell Filter by specialty or product code using the sidebar.
Cadwell — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jul 23, 2014
CADWELL SPIKE AND SEIZURE DETECTOR
Neurology
141d
Cleared
Mar 19, 2013
CADWELL DISPOSABLE PROBE HANDLE
Neurology
118d