FDA 510(k) Application Details - K033674

Device Classification Name	Assay, Glycosylated Hemoglobin   More FDA Info for this Device
510(K) Number	K033674
Device Name	Assay, Glycosylated Hemoglobin
Applicant	SERADYN INC. 7998 GEORGETOWN RD. SUITE 1000 INDIANAPOLIS, IN 46268-5260 US Other 510(k) Applications for this Company
Contact	LES PADILLA Other 510(k) Applications for this Contact
Regulation Number	864.7470   More FDA Info for this Regulation Number
Classification Product Code	LCP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/24/2003
Decision Date	02/09/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review