FDA 510(k) Application Details - K062234

Device Classification Name	Test, System, Immunoassay, Lipoprotein-Associated Phospholipase A2   More FDA Info for this Device
510(K) Number	K062234
Device Name	Test, System, Immunoassay, Lipoprotein-Associated Phospholipase A2
Applicant	DIADEXUS, INC. 343 OYSTER POINT BLVD. SOUTH SAN FRANCISCO, CA 94080 US Other 510(k) Applications for this Company
Contact	ROBERT L WOLFERT Other 510(k) Applications for this Contact
Regulation Number	866.5600   More FDA Info for this Regulation Number
Classification Product Code	NOE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2006
Decision Date	09/11/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
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