FDA 510(k) Application Details - K022533

Device Classification Name	Calibrator, Secondary   More FDA Info for this Device
510(K) Number	K022533
Device Name	Calibrator, Secondary
Applicant	Qualigen, Inc. 2042 CORTE DEL NOGAL CARLSBAD, CA 92009 US Other 510(k) Applications for this Company
Contact	DOROTHY DEINZER Other 510(k) Applications for this Contact
Regulation Number	862.1150   More FDA Info for this Regulation Number
Classification Product Code	JIT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/2002
Decision Date	09/30/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review