FDA 510(k) Application Details - K061573

Device Classification Name	Transducer, Blood-Pressure, Extravascular   More FDA Info for this Device
510(K) Number	K061573
Device Name	Transducer, Blood-Pressure, Extravascular
Applicant	HOSPIRA, INC. 275 NORTH FIELD DR. LAKE FOREST, IL 60045 US Other 510(k) Applications for this Company
Contact	THOMAS KOZMA Other 510(k) Applications for this Contact
Regulation Number	870.2850   More FDA Info for this Regulation Number
Classification Product Code	DRS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/07/2006
Decision Date	09/19/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review