FDA 510(k) Application Details - K181012

Device Classification Name	Calprotectin, Fecal   More FDA Info for this Device
510(K) Number	K181012
Device Name	Calprotectin, Fecal
Applicant	BUHLMANN Laboratories AG Baselstrasse 55 Schonenbuch CH-4124 CH Other 510(k) Applications for this Company
Contact	Alicja Ritz Other 510(k) Applications for this Contact
Regulation Number	866.5180   More FDA Info for this Regulation Number
Classification Product Code	NXO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/17/2018
Decision Date	06/04/2018
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