FDA 510(k) Application Details - K023784

Device Classification Name	Ldl & Vldl Precipitation, Hdl   More FDA Info for this Device
510(K) Number	K023784
Device Name	Ldl & Vldl Precipitation, Hdl
Applicant	HEMAGEN DIAGNOSTICS, INC. 9033 RED BRANCH RD. COLUMBIA, MD 21045 US Other 510(k) Applications for this Company
Contact	JOSE A MONTANEZ Other 510(k) Applications for this Contact
Regulation Number	862.1475   More FDA Info for this Regulation Number
Classification Product Code	LBR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/12/2002
Decision Date	12/24/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review