FDA 510(k) Application Details - K001129

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K001129
Device Name	Anesthesia Conduction Kit
Applicant	LIFE-TECH INTL., 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	868.5140   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	04/07/2000
Decision Date	07/06/2000
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