Rudolf Storz GmbH is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Rudolf Storz GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Rudolf Storz GmbH has 1 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Rudolf Storz GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rudolf Storz GmbH
1 devices