FDA 510(k) Application Details - K012131

Device Classification Name	Enzyme Immunoassay, Benzodiazipine   More FDA Info for this Device
510(K) Number	K012131
Device Name	Enzyme Immunoassay, Benzodiazipine
Applicant	PAN PROBE BIOTECH, INC. 8515 ARJONS DR., SUITE A SAN DIEGO, CA 92126 US Other 510(k) Applications for this Company
Contact	ALICE H YU Other 510(k) Applications for this Contact
Regulation Number	862.3170   More FDA Info for this Regulation Number
Classification Product Code	JXM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/09/2001
Decision Date	07/20/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	TX - Clinical Toxicology
Review Advisory Committee	TX - Clinical Toxicology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review