FDA 510(k) Application Details - K081074

Device Classification Name	Radioimmunoassay, Thyroid-Stimulating Hormone   More FDA Info for this Device
510(K) Number	K081074
Device Name	Radioimmunoassay, Thyroid-Stimulating Hormone
Applicant	Siemens Healthcare Diagnostics Inc. PO BOX 6101 MAILBOX 514 NEWARK, DE 19714-6101 US Other 510(k) Applications for this Company
Contact	YUK-TING LEWIS Other 510(k) Applications for this Contact
Regulation Number	862.1690   More FDA Info for this Regulation Number
Classification Product Code	JLW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/16/2008
Decision Date	05/23/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review