Medical Device Manufacturer · NL , Nl-3981 La Bunnik

Erich Jaeger B.V. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1998

Total

Cleared

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

1-3 of 3