FDA 510(k) Application Details - K041753

Device Classification Name	Extractable Antinuclear Antibody, Antigen And Control   More FDA Info for this Device
510(K) Number	K041753
Device Name	Extractable Antinuclear Antibody, Antigen And Control
Applicant	AESKU.DIAGNOSTICS 8880 NW 18TH TERRACE MIAMI, FL 33172 US Other 510(k) Applications for this Company
Contact	STANLEY AMMONS Other 510(k) Applications for this Contact
Regulation Number	866.5100   More FDA Info for this Regulation Number
Classification Product Code	LLL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/29/2004
Decision Date	07/14/2004
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	N
Expedited Review