Thyssenkrupp Accessibility B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Thyssenkrupp Accessibility B.V. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Thyssenkrupp Accessibility B.V. has 2 FDA 510(k) cleared medical devices. Based in Zuid-Holland, NL.
Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Thyssenkrupp Accessibility B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thyssenkrupp Accessibility B.V.
2 devices