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FDA 510(k) Application Details - K050590
Device Classification Name
Enzyme Linked Immunoabsorption Assay, Treponema Pallidum
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510(K) Number
K050590
Device Name
Enzyme Linked Immunoabsorption Assay, Treponema Pallidum
Applicant
DIESSE DIAGNOSTICA SENESE S.P.A
555 NE 34TH ST #1905
MIAMI, FL 33137 US
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Contact
GLORIA SCHLANSER
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Regulation Number
866.3830
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Classification Product Code
LIP
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More FDA Info for this Product Code
Date Received
03/08/2005
Decision Date
08/10/2006
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
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