FDA 510(k) Application Details - K101572

Device Classification Name	System, Test, Radioallergosorbent (Rast) Immunological   More FDA Info for this Device
510(K) Number	K101572
Device Name	System, Test, Radioallergosorbent (Rast) Immunological
Applicant	SIEMENS HEALTHCARE DIAGNOSTICS 511 benedict Avenue Tarrytown, NY 10591 US Other 510(k) Applications for this Company
Contact	CLARE SANTULLI Other 510(k) Applications for this Contact
Regulation Number	866.5750   More FDA Info for this Regulation Number
Classification Product Code	DHB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2010
Decision Date	08/01/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review