FDA 510(k) Application Details - K033738

Device Classification Name	Computer, Blood-Pressure   More FDA Info for this Device
510(K) Number	K033738
Device Name	Computer, Blood-Pressure
Applicant	SCHILLER AG ALTGASSE 68 BAAR CH-6341 CH Other 510(k) Applications for this Company
Contact	MARKUS BUETLER Other 510(k) Applications for this Contact
Regulation Number	870.1110   More FDA Info for this Regulation Number
Classification Product Code	DSK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/28/2003
Decision Date	08/24/2004
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	N
Expedited Review