Mindray North America is one of 5122 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
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.
Mindray North America — FDA 510(k) Products and Clearance History
3 devices
Cleared
May 16, 2014
VITAL SIGNS MONITOR
Cardiovascular
319d
Cleared
May 02, 2014
ACCUTORR 7 VITAL SIGNS MONITOR
Cardiovascular
305d
Cleared
Apr 18, 2014
PASSPORT M SERIES PATIENT MONITORING (INCLUDING MODELS PASSPORT 17M AND...
Cardiovascular
289d