FDA 510(k) Application Details - K041002

Device Classification Name	Antibodies, Gliadin   More FDA Info for this Device
510(K) Number	K041002
Device Name	Antibodies, Gliadin
Applicant	BIOMEDICAL DIAGNOSTICS S.A. ACTIPOLE, 25-BD DE BEAUBOURG BP 103 MARNE-LA-VALLEE, CEDEX 2 77423 FR Other 510(k) Applications for this Company
Contact	PASCALE LAROCHE Other 510(k) Applications for this Contact
Regulation Number	866.5750   More FDA Info for this Regulation Number
Classification Product Code	MST Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/19/2004
Decision Date	09/24/2004
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