FDA 510(k) Application Details - K093662

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K093662
Device Name	Anesthesia Conduction Kit
Applicant	LIFE-TECH, INC. 13235 NORTH PROMENADE BLVD. STAFFORD, TX 77477 US Other 510(k) Applications for this Company
Contact	JEFF KASOFF Other 510(k) Applications for this Contact
Regulation Number	868.5140   More FDA Info for this Regulation Number
Classification Product Code	CAZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/25/2009
Decision Date	06/24/2010
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