FDA 510(k) Application Details - K101319

Device Classification Name	Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control   More FDA Info for this Device
510(K) Number	K101319
Device Name	Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control
Applicant	IMMCO DIAGNOSTICS, INC. 60 PINEVIEW DR. BUFFALO, NY 14228-2120 US Other 510(k) Applications for this Company
Contact	KEVIN LAWSON Other 510(k) Applications for this Contact
Regulation Number	866.5100   More FDA Info for this Regulation Number
Classification Product Code	LRM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/11/2010
Decision Date	12/09/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	Y
Expedited Review