Winprobe Corporation is one of 19028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Winprobe Corporation - FDA 510(k) Cleared Devices
Recent clearances: UltraVision 2 Diagnostic Ultrasound System, UltraVision 2 Diagnostic Ultrasound System
2
Total
2
Cleared
0
Denied
Winprobe Corporation has 2 FDA 510(k) cleared medical devices. Based in Palm Beach Gradens, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Winprobe 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 - Winprobe Corporation
2 devices