FDA 510(k) Application Details - K954953

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K954953
Device Name	Anesthesia Conduction Kit
Applicant	BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC ONE BECTON DR. FRANKLIN LAKES, NJ 07417-1880 US Other 510(k) Applications for this Company
Contact	GREGORY W MORGAN 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	10/30/1995
Decision Date	05/20/1996
Decision	SESK - SUBST EQUIV - KIT
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review