FDA 510(k) Application Details - K950672

Device Classification Name	Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus   More FDA Info for this Device
510(K) Number	K950672
Device Name	Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus
Applicant	DIAGNOSTIC PRODUCTS CORP. 5700 WEST 96TH ST. LOS ANGELES, CA 90045-5597 US Other 510(k) Applications for this Company
Contact	KEN ASARCH Other 510(k) Applications for this Contact
Regulation Number	866.3175   More FDA Info for this Regulation Number
Classification Product Code	LFZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/13/1995
Decision Date	06/17/1996
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