FDA 510(k) Application Details - K011952

Device Classification Name	Enzyme Immunoassay, Amphetamine   More FDA Info for this Device
510(K) Number	K011952
Device Name	Enzyme Immunoassay, Amphetamine
Applicant	MICRODIAGNOSTICS, INC. 28062 FORBES ROAD, SUITE B LAGUNA NIGUEL, CA 92677 US Other 510(k) Applications for this Company
Contact	JUNE SHOZI 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	06/21/2001
Decision Date	10/25/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review