Aiq Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aiq Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Quantitative Total Extensible Imaging (QTxI)
1
Total
1
Cleared
0
Denied
Aiq Solutions, Inc. has 1 FDA 510(k) cleared medical devices. Based in Madison, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aiq Solutions, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Epireg, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Aiq Solutions, Inc.
1 devices