FDA 510(k) Application Details - K081975

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K081975
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	ABBOTT DIABETES CARE INC. 1360 SOUTH LOOP RD. ALAMEDA, CA 94502 US Other 510(k) Applications for this Company
Contact	ARUL STERLIN 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	07/11/2008
Decision Date	11/26/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
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