FDA 510(k) Application Details - K171083

Device Classification Name	Method, Enzymatic, Glucose (Urinary, Non-Quantitative)   More FDA Info for this Device
510(K) Number	K171083
Device Name	Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Applicant	Iris Diagnostics, a Division of Iris International Inc 9172 Eton Avenue Chatsworth, CA 91311 US Other 510(k) Applications for this Company
Contact	Nancy Nadler Other 510(k) Applications for this Contact
Regulation Number	862.1340   More FDA Info for this Regulation Number
Classification Product Code	JIL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/11/2017
Decision Date	05/12/2017
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
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