FDA 510(k) Application Details - K072050

Device Classification Name	Catheter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K072050
Device Name	Catheter, Conduction, Anesthetic
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	868.5120   More FDA Info for this Regulation Number
Classification Product Code	BSO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/26/2007
Decision Date	10/18/2007
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