510(k) K925640

XOMED-TREACE EMG ENDOTRACHEAL TUBEEN by Xomed-Treace, Inc. — Product Code ETN

K925640 is an FDA 510(k) premarket notification submitted by Xomed-Treace, Inc. for the device "XOMED-TREACE EMG ENDOTRACHEAL TUBEEN". The FDA issued a decision of Substantially Equivalent on August 17, 1993. The device falls under product code ETN (Stimulator, Nerve), a Class II device regulated under 21 CFR 874.1820. Xomed-Treace, Inc. has at least 10 other 510(k) clearances on record.