FDA 510(k) Application Details - K100024

Device Classification Name	Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)   More FDA Info for this Device
510(K) Number	K100024
Device Name	Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)
Applicant	TECO DIAGNOSTICS 1268 NORTH LAKEVIEW AVE. ANAHEIM, CA 92807 US Other 510(k) Applications for this Company
Contact	KC CHEN Other 510(k) Applications for this Contact
Regulation Number	862.1510   More FDA Info for this Regulation Number
Classification Product Code	JMT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/05/2010
Decision Date	02/17/2011
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