Ultralinq Healthcare Solutions, Inc. is one of 16403 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ultralinq Healthcare Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UltraLinq
1
Total
1
Cleared
0
Denied
Ultralinq Healthcare Solutions, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ultralinq Healthcare Solutions, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MethodSense, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ultralinq Healthcare Solutions, Inc.
1 devices