FDA 510(k) Application Details - K032144

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K032144
Device Name	Anesthesia Conduction Kit
Applicant	B. BRAUN MEDICAL, INC. 901 MARCON BLVD. ALLENTOWN, PA 18109-9341 US Other 510(k) Applications for this Company
Contact	AMY SMITH 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	07/14/2003
Decision Date	10/01/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review