FDA 510(k) Application Details - K123983

Device Classification Name	System, Test, Vitamin D   More FDA Info for this Device
510(K) Number	K123983
Device Name	System, Test, Vitamin D
Applicant	Qualigen, Inc. 2042 CORTE DEL NOGAL SUITE B CARLSBAD, CA 92011-1438 US Other 510(k) Applications for this Company
Contact	MICHAEL S POIRIER Other 510(k) Applications for this Contact
Regulation Number	862.1825   More FDA Info for this Regulation Number
Classification Product Code	MRG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/26/2012
Decision Date	07/03/2013
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