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FDA 510(k) Application Details - K111107
Device Classification Name
Powder, Porcelain
More FDA Info for this Device
510(K) Number
K111107
Device Name
Powder, Porcelain
Applicant
NORITAKE CO., INC.
700 12 STREET, N.W.,
SUITE 1100
WASHINGTON, DC 20005 US
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Contact
IVAN WASSERMAN
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Regulation Number
872.6660
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Classification Product Code
EIH
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More FDA Info for this Product Code
Date Received
04/20/2011
Decision Date
06/30/2011
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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