Leibinger & Fischer , Ltd.

Leibinger & Fischer , Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 1990, most recent 1991.

Top product codes for Leibinger & Fischer , Ltd.

GXD — Neurology1 device
IYE — Radiology1 device

Recent clearances by Leibinger & Fischer , Ltd.

K896450 — NEURO N 50 LESION GENERATORCode GXD·1991-03-19
K892425 — STP COMPLETE MODULE SETCode IYE·1990-03-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.