FDA 510(k) Application Details - K052115

Device Classification Name	Enzyme Immunoassay, Amphetamine   More FDA Info for this Device
510(K) Number	K052115
Device Name	Enzyme Immunoassay, Amphetamine
Applicant	FIRST CHECK DIAGNOSTICS LLC 13 SPECTRUM POINTE DR. LAKE FOREST, CA 92630 US Other 510(k) Applications for this Company
Contact	KEVIN J GADAWSKI Other 510(k) Applications for this Contact
Regulation Number	862.3100   More FDA Info for this Regulation Number
Classification Product Code	DKZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/04/2005
Decision Date	12/29/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review