Medqia is one of 24579 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medqia - FDA 510(k) Cleared Devices
Recent clearances: IBIS EXPLORER AND MARKUP SOFTWARE
1
Total
1
Cleared
0
Denied
Medqia has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medqia Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medqia
1 devices