Qisda Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Qisda Corporation - FDA 510(k) Cleared Devices
Recent clearances: InnoSight Diagnostic Ultrasound System, BenQ Diagnostic Ultrasound System
4
Total
4
Cleared
0
Denied
Qisda Corporation has 4 FDA 510(k) cleared medical devices. Based in Dublin, US.
Historical record: 4 cleared submissions from 2014 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Qisda Corporation 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 - Qisda Corporation
4 devices