FDA 510(k) Application Details - K953118

Device Classification Name	Apparatus, Autotransfusion   More FDA Info for this Device
510(K) Number	K953118
Device Name	Apparatus, Autotransfusion
Applicant	MEDTRONIC VASCULAR 18501 EAST PLAZA DR. PARKER, CO 80134-9061 US Other 510(k) Applications for this Company
Contact	KENNETH E IMLER Other 510(k) Applications for this Contact
Regulation Number	868.5830   More FDA Info for this Regulation Number
Classification Product Code	CAC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/03/1995
Decision Date	02/23/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review