Kineticor, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kineticor, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Motion Correction System
1
Total
1
Cleared
0
Denied
Kineticor, Inc. has 1 FDA 510(k) cleared medical devices. Based in Honolulu, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Kineticor, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kineticor, Inc.
1 devices