FDA 510(k) Application Details - K962880

Device Classification Name	Anesthesia Conduction Kit   More FDA Info for this Device
510(K) Number	K962880
Device Name	Anesthesia Conduction Kit
Applicant	SHERWOOD MEDICAL CO. 1915 OLIVE ST. ST. LOUIS, MO 63103-1642 US Other 510(k) Applications for this Company
Contact	DENNIS POZZO 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	07/24/1996
Decision Date	12/09/1996
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