Neuro Kinetics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neuro Kinetics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: I-Portal Neuro Otologic Test Center
3
Total
3
Cleared
0
Denied
Neuro Kinetics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 3 cleared submissions from 2015 to 2018. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Neuro Kinetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neuro Kinetics, Inc.
3 devices