510(k) K012077

IMMULITE RUBELLA IGM,LKRM1, LKRM2, IMMULITE 2000 RUBELLA IGM, MODEL L2KRM2, L2KRM6 by Diagnostic Products Corp. — Product Code LFX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 10, 2002
Date Received
July 2, 2001
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Rubella
Device Class
Class II
Regulation Number
866.3510
Review Panel
MI
Submission Type