FDA 510(k) Application Details - K081864

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K081864
Device Name	Needle, Conduction, Anesthetic (W/Wo Introducer)
Applicant	LIFE-TECH, INC. 4235 GREENBRIAR DR. STAFFORD, TX 77477-3995 US Other 510(k) Applications for this Company
Contact	JEFF KASOFF Other 510(k) Applications for this Contact
Regulation Number	868.5150   More FDA Info for this Regulation Number
Classification Product Code	BSP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/01/2008
Decision Date	09/25/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review