FDA 510(k) Application Details - K012636

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K012636
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	VSM TECHNOLOGY, INC. 675 WEST HASTING ST., 15TH FL. VANCOUVER, B.C. V6B 1N2 CA Other 510(k) Applications for this Company
Contact	DARYL WISDAHL 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	08/13/2001
Decision Date	10/26/2001
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