FDA 510(k) Application Details - K960085

Device Classification Name	Calibrator, Multi-Analyte Mixture   More FDA Info for this Device
510(K) Number	K960085
Device Name	Calibrator, Multi-Analyte Mixture
Applicant	ALKO DIAGNOSTIC CORP. 333 FISKE ST. HOLLISTON, MA 01746 US Other 510(k) Applications for this Company
Contact	JANET A MCGRATH 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	01/11/1996
Decision Date	03/11/1996
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