FDA 510(k) Application Details - K960888

Device Classification Name	Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)   More FDA Info for this Device
510(K) Number	K960888
Device Name	Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)
Applicant	BAYER CORP. 1884 MILES AVE. ELKHART, IN 46514 US Other 510(k) Applications for this Company
Contact	ROSANNE M SAVOL 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	03/04/1996
Decision Date	07/05/1996
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