FDA 510(k) Application Details - K050499

Device Classification Name	Needle, Conduction, Anesthetic (W/Wo Introducer)   More FDA Info for this Device
510(K) Number	K050499
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	02/28/2005
Decision Date	05/17/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review