Cyberlogic, Inc. is one of 22007 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cyberlogic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UltraScan 650
1
Total
1
Cleared
0
Denied
Cyberlogic, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cyberlogic, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Promedic, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cyberlogic, Inc.
1 devices