FDA 510(k) Application Details - K132072

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K132072
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	NIPRO DIAGNOSTICS, INC. 2400 NW 55TH COURT Fort Lauderdale, FL 33309 US Other 510(k) Applications for this Company
Contact	BETH FOSTER 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	07/03/2013
Decision Date	08/15/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
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