Medical Device Manufacturer · US , Dallas , TX

Leibinger & Fischer , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990
2
Total
2
Cleared
0
Denied

Leibinger & Fischer , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Dallas, US.

Historical record: 2 cleared submissions from 1990 to 1991. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Leibinger & Fischer , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Leibinger & Fischer , Ltd.
2 devices
1-2 of 2
Filters