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FDA 510(k) Application Details - K983470
Device Classification Name
Powder, Porcelain
More FDA Info for this Device
510(K) Number
K983470
Device Name
Powder, Porcelain
Applicant
NORITAKE CO., INC.
1050 CONNECTICUT AVENUE, N.W.
WASHINGTON, DC 20036-5339 US
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Contact
MARSHA C WERTZBERGER
Other 510(k) Applications for this Contact
Regulation Number
872.6660
More FDA Info for this Regulation Number
Classification Product Code
EIH
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/01/1998
Decision Date
12/22/1998
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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