FDA 510(k) Application Details - K063186

Device Classification Name Enzyme Linked Immunoabsorbent Assay, Rubella

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510(K) Number K063186
Device Name Enzyme Linked Immunoabsorbent Assay, Rubella
Applicant ZEUS SCIENTIFIC, INC.
P.O. BOX 38
RARITAN, NJ 08869 US
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Contact EWA NADOLCZAK
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Regulation Number 866.3510

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Classification Product Code LFX
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Date Received 10/20/2006
Decision Date 03/21/2007
Decision SESE - SUBST EQUIV
Classification Advisory Committee MI - Microbiology
Review Advisory Committee MI - Microbiology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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