Medical Device Manufacturer · US , Washington , DC

Leibinger GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Leibinger GmbH Neurology ✕

1 devices

1-1 of 1

Cleared Sep 01, 1995

LEIBINGER STEREOPLAN PLUS STEROTACTIC TREATMENT PLAN ING SOFTWARE PACKAGE

Neurology · 266d