FDA 510(k) Application Details - K991719

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K991719
Device Name	Anesthesia Conduction Kit
Applicant	MEDIMEX HOLFELD GMBH & CO. MID VALLEY PROFESSIONAL PLAZA SALT LAKE CITY, UT 84047-7101 US Other 510(k) Applications for this Company
Contact	DONALD F GRABARZ 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	05/20/1999
Decision Date	08/18/1999
Decision	SESK - SUBST EQUIV - KIT
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review