Mindray North America is one of 19082 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mindray North America - FDA 510(k) Cleared Devices
Recent clearances: VITAL SIGNS MONITOR, ACCUTORR 7 VITAL SIGNS MONITOR, PASSPORT M SERIES PATIENT MONITORING (INCLUDING MODELS PASSPORT 17M AND PASSPORT 12M)
3
Total
3
Cleared
0
Denied
Mindray North America has 3 FDA 510(k) cleared medical devices. Based in Mahwh, US.
Historical record: 3 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mindray North America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mindray North America
3 devices