Qisda Corporation is one of 12759 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, InnoSight 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.
Regulatory submissions have been managed by Leiker Regulatory & Quality Consulting and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Qisda Corporation
4 devices