FDA 510(k) Application Details - K023015

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K023015
Device Name	Computer, Diagnostic, Programmable
Applicant	SCHWARZER GMBH BAERMANNSTRASSE 38 MUNICH D-81245 DE Other 510(k) Applications for this Company
Contact	EIKE KINZEL Other 510(k) Applications for this Contact
Regulation Number	870.1425   More FDA Info for this Regulation Number
Classification Product Code	DQK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/10/2002
Decision Date	09/25/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review