FDA 510(k) Application Details - K051452

Device Classification Name	Calibrator, Multi-Analyte Mixture   More FDA Info for this Device
510(K) Number	K051452
Device Name	Calibrator, Multi-Analyte Mixture
Applicant	SENTINEL CH. SRL 5 VIA PRINCIPE EUGENIO MILANO 20155 IT Other 510(k) Applications for this Company
Contact	DAVIDE SPADA Other 510(k) Applications for this Contact
Regulation Number	862.1150   More FDA Info for this Regulation Number
Classification Product Code	JIX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/02/2005
Decision Date	10/25/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review