FDA 510(k) Application Details - K083339

Device Classification Name	Cresolphthalein Complexone, Calcium   More FDA Info for this Device
510(K) Number	K083339
Device Name	Cresolphthalein Complexone, Calcium
Applicant	Siemens Healthcare Diagnostics Inc. 511 BENEDICT AVENUE TARRYTOWN, NY 10509 US Other 510(k) Applications for this Company
Contact	Lubomyr Shchur Other 510(k) Applications for this Contact
Regulation Number	862.1145   More FDA Info for this Regulation Number
Classification Product Code	CIC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/12/2008
Decision Date	03/09/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review