FDA 510(k) Application Details - K121468

Device Classification Name	Multi-Analyte Controls, All Kinds (Assayed)   More FDA Info for this Device
510(K) Number	K121468
Device Name	Multi-Analyte Controls, All Kinds (Assayed)
Applicant	EUROTROL B.V. KEPLERLAAN 20 EDE 6716 BS NL Other 510(k) Applications for this Company
Contact	PAUL B.P. KOOIJMANS Other 510(k) Applications for this Contact
Regulation Number	862.1660   More FDA Info for this Regulation Number
Classification Product Code	JJY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/17/2012
Decision Date	06/22/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review