FDA 510(k) Application Details - K993961

Device Classification Name	Enzyme Immunoassay, Cannabinoids   More FDA Info for this Device
510(K) Number	K993961
Device Name	Enzyme Immunoassay, Cannabinoids
Applicant	AMERICAN BIO MEDICA CORP. 122 SMITH RD. KINDERHOOK, NY 12106 US Other 510(k) Applications for this Company
Contact	HENRY WELLS 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	11/22/1999
Decision Date	01/24/2000
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	N
Expedited Review