Swissray Medical AG is one of 19020 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Swissray Medical AG - FDA 510(k) Cleared Devices
Recent clearances: DDRCRUZE (DIGITAL MOBILE DIAGNOSTIC X-RAY SYSTEM), DDRVERSA MOTION, DDRELEMENT
4
Total
4
Cleared
0
Denied
Swissray Medical AG has 4 FDA 510(k) cleared medical devices. Based in Elizabeth, US.
Historical record: 4 cleared submissions from 2005 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Swissray Medical AG 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 - Swissray Medical AG
4 devices