FDA 510(k) Application Details - K060380

Device Classification Name	Anti-Dna Antibody, Antigen And Control   More FDA Info for this Device
510(K) Number	K060380
Device Name	Anti-Dna Antibody, Antigen And Control
Applicant	BIOMEDICAL DIAGNOSTICS (BMD) SA ACTIPOLE 25 4-6 BLD DE BEAUBOURG MARNE LA VALLEE CEDEX 2 77435 FR Other 510(k) Applications for this Company
Contact	CHRISTELLE COURIVAUD Other 510(k) Applications for this Contact
Regulation Number	866.5100   More FDA Info for this Regulation Number
Classification Product Code	LSW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/14/2006
Decision Date	05/02/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	IM - Immunology
Review Advisory Committee	IM - Immunology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review