FDA 510(k) Application Details - K040410

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K040410
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	A C COSSOR & SON (SURGICAL) LIMITED VALE ROAD LONDON N4 1PS GB Other 510(k) Applications for this Company
Contact	A J COSSOR Other 510(k) Applications for this Contact
Regulation Number	870.1130   More FDA Info for this Regulation Number
Classification Product Code	DXN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/18/2004
Decision Date	05/05/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review