FDA 510(k) Application Details - K110780

Device Classification Name	Diazo Colorimetry, Bilirubin   More FDA Info for this Device
510(K) Number	K110780
Device Name	Diazo Colorimetry, Bilirubin
Applicant	ELITECH GROUP 21720 23RD DR S.E., SUITE 150 BOTHELL, WA 98021 US Other 510(k) Applications for this Company
Contact	DEBRA K HUTSON Other 510(k) Applications for this Contact
Regulation Number	862.1110   More FDA Info for this Regulation Number
Classification Product Code	CIG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/21/2011
Decision Date	10/07/2011
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