FDA 510(k) Application Details - K010001

Device Classification Name	Enzyme Immunoassay, Cannabinoids   More FDA Info for this Device
510(K) Number	K010001
Device Name	Enzyme Immunoassay, Cannabinoids
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	862.3870   More FDA Info for this Regulation Number
Classification Product Code	LDJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/02/2001
Decision Date	02/05/2001
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