FDA 510(k) Application Details - K093987

Device Classification Name	System, Test, Radioallergosorbent (Rast) Immunological   More FDA Info for this Device
510(K) Number	K093987
Device Name	System, Test, Radioallergosorbent (Rast) Immunological
Applicant	Siemens Healthcare Diagnostics Inc. 5210 PACIFIC CONCOURSE DRIVE LOS ANGELES, CA 90045 US Other 510(k) Applications for this Company
Contact	DONNA VELASQUEZ 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	12/24/2009
Decision Date	03/28/2011
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