FDA 510(k) Application Details - K954706

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K954706
Device Name	Anesthesia Conduction Kit
Applicant	KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH 15 HAMPSHIRE ST. MANSFIELD, MA 02048 US Other 510(k) Applications for this Company
Contact	DAVID A OLSON 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	10/12/1995
Decision Date	05/30/1996
Decision	SESD - SUBST EQUIV - WITH DRUG
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review