FDA 510(k) Application Details - K052989

Device Classification Name	Probe, Blood-Flow, Extravascular   More FDA Info for this Device
510(K) Number	K052989
Device Name	Probe, Blood-Flow, Extravascular
Applicant	DELTEX MEDICAL TERMINUS RD. CHICHESTER, WEST SUSSEX PO19 8TX GB Other 510(k) Applications for this Company
Contact	LAWRENCE BROOKFIELD Other 510(k) Applications for this Contact
Regulation Number	870.2120   More FDA Info for this Regulation Number
Classification Product Code	DPT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/24/2005
Decision Date	03/08/2006
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