FDA 510(k) Application Details - K110435

Device Classification Name	System, Test, Blood Glucose, Over The Counter   More FDA Info for this Device
510(K) Number	K110435
Device Name	System, Test, Blood Glucose, Over The Counter
Applicant	US DIAGNOSTICS, INC. 304 PARK AVENUE SOUTH SUITE 218 NEW YORK, NY 10010-4301 US Other 510(k) Applications for this Company
Contact	JONATHAN JOHNSON 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	02/15/2011
Decision Date	09/21/2011
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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