Fischer-Zoth Audiologic Systems, Inc.

Fischer-Zoth Audiologic Systems, Inc. holds 2 FDA 510(k) medical device clearances, first cleared 1998, most recent 2002.

Top product codes for Fischer-Zoth Audiologic Systems, Inc.

EWO — Ear, Nose, Throat1 device
GWJ — Neurology1 device

Recent clearances by Fischer-Zoth Audiologic Systems, Inc.

K013977 — ECHO-SCREEN T, TA, TD, TDA, TCCode GWJ·2002-06-14
K982642 — ECHO-SCREENCode EWO·1998-10-21

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