Mindray DS USA, Inc. is one of 18365 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mindray DS USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: V SERIES MONITORING SYSTEM, 12.1 DCU/V12 AND 21.0 DCU/V21, AS3700 ANESTHSIA DELIVERY SYSTEM, ENDEAVOUR MONITORING SYSTEM
3
Total
3
Cleared
0
Denied
Mindray DS USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mahwh, US.
Historical record: 3 cleared submissions from 2010 to 2013.
Browse the FDA 510(k) cleared devices submitted by Mindray DS USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mindray DS USA, Inc.
3 devices