Erich Jaeger B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Erich Jaeger B.V. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Erich Jaeger B.V. has 3 FDA 510(k) cleared medical devices. Based in Nl-3981 La Bunnik, NL.
Historical record: 3 cleared submissions from 1998 to 2000. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Erich Jaeger B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Erich Jaeger B.V.
3 devices