FDA 510(k) Application Details - K173792

Device Classification Name	Test System, Antineutrophil Cytoplasmic Antibodies (Anca)   More FDA Info for this Device
510(K) Number	K173792
Device Name	Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
Applicant	Phadia AB Rapsgatan 7P Uppsala SE 754 50 SE Other 510(k) Applications for this Company
Contact	Carina Magnusson Other 510(k) Applications for this Contact
Regulation Number	866.5660   More FDA Info for this Regulation Number
Classification Product Code	MOB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/14/2017
Decision Date	03/13/2018
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