FDA 510(k) Application Details - K954920

Device Classification Name	Latex Agglutination Assay, Rubella   More FDA Info for this Device
510(K) Number	K954920
Device Name	Latex Agglutination Assay, Rubella
Applicant	MUREX DIAGNOSTICS, INC. 3075 NORTHWOODS CIR. NORCROSS, GA 30071-1542 US Other 510(k) Applications for this Company
Contact	ROBERT K SHOCKLEY Other 510(k) Applications for this Contact
Regulation Number	866.3510   More FDA Info for this Regulation Number
Classification Product Code	LQN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/26/1995
Decision Date	08/21/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review