Compumedics USA, Ltd. is one of 24259 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Compumedics USA, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: COMPUMEDICS NEUVO, COMPUMEDICS SUMMIT IP, CONDUCTIVE EEG ELECTROLYTE
3
Total
3
Cleared
0
Denied
Compumedics USA, Ltd. has 3 FDA 510(k) cleared medical devices. Based in El Paso, US.
Historical record: 3 cleared submissions from 2003 to 2008. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Compumedics USA, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Compumedics USA, Ltd.
3 devices