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FDA 510(k) Application Details - K082085
Device Classification Name
Immunoelectrophoretic, Immunoglobulins, (G, A, M)
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510(K) Number
K082085
Device Name
Immunoelectrophoretic, Immunoglobulins, (G, A, M)
Applicant
SEBIA
400-1705 CORPORATE DRIVE
SUITE 400
NORCROSS, GA 30093 US
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Contact
KAREN ANDERSON
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Regulation Number
866.5510
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Classification Product Code
CFF
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More FDA Info for this Product Code
Date Received
07/23/2008
Decision Date
04/17/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
IM - Immunology
Review Advisory Committee
IM - Immunology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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