FDA 510(k) Application Details - K021819

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K021819
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	LIFESCAN, INC. 1000 GIBRALTAR DR. MILPITAS, CA 95035-6312 US Other 510(k) Applications for this Company
Contact	MARY ELLEN HOLDEN Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	NBW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2002
Decision Date	08/23/2002
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