FDA 510(k) Application Details - K050590

Device Classification Name	Enzyme Linked Immunoabsorption Assay, Treponema Pallidum   More FDA Info for this Device
510(K) Number	K050590
Device Name	Enzyme Linked Immunoabsorption Assay, Treponema Pallidum
Applicant	DIESSE DIAGNOSTICA SENESE S.P.A 555 NE 34TH ST #1905 MIAMI, FL 33137 US Other 510(k) Applications for this Company
Contact	GLORIA SCHLANSER Other 510(k) Applications for this Contact
Regulation Number	866.3830   More FDA Info for this Regulation Number
Classification Product Code	LIP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/08/2005
Decision Date	08/10/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review