SUPER PORCELAIN STAIN- PURE WHITE

Powder, Porcelain

NORITAKE CO., INC.

The following data is part of a premarket notification filed by Noritake Co., Inc. with the FDA for Super Porcelain Stain- Pure White.

Pre-market Notification Details

Device IDK983470
510k NumberK983470
Device Name:SUPER PORCELAIN STAIN- PURE WHITE
ClassificationPowder, Porcelain
Applicant NORITAKE CO., INC. 1050 CONNECTICUT AVENUE, N.W. Washington,  DC  20036 -5339
ContactMarsha C Wertzberger
CorrespondentMarsha C Wertzberger
NORITAKE CO., INC. 1050 CONNECTICUT AVENUE, N.W. Washington,  DC  20036 -5339
Product CodeEIH  
CFR Regulation Number872.6660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1998-10-01
Decision Date1998-12-22

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
EKUR1023451KA0 K983470 000
EKUR1023571KA0 K983470 000
EKUR1023581KA0 K983470 000
EKUR1023591KA0 K983470 000
EKUR1023601KA0 K983470 000
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EKUR1023631KA0 K983470 000
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EKUR1023651KA0 K983470 000
EKUR1023561KA0 K983470 000
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EKUR1023471KA0 K983470 000
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EKUR1023491KA0 K983470 000
EKUR1023501KA0 K983470 000
EKUR1023511KA0 K983470 000
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EKUR1023531KA0 K983470 000
EKUR1023541KA0 K983470 000
EKUR1023661KA0 K983470 000
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EKUR1023811KA0 K983470 000
EKUR1023821KA0 K983470 000
EKUR1023831KA0 K983470 000
EKUR1023841KA0 K983470 000
EKUR1023851KA0 K983470 000
EKUR1023861KA0 K983470 000
EKUR1020220KA0 K983470 000
EKUR1023781KA0 K983470 000
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EKUR1023681KA0 K983470 000
EKUR1023691KA0 K983470 000
EKUR1023701KA0 K983470 000
EKUR1023711KA0 K983470 000
EKUR1023721KA0 K983470 000
EKUR1023731KA0 K983470 000
EKUR1023741KA0 K983470 000
EKUR1023751KA0 K983470 000
EKUR1023761KA0 K983470 000
EKUR1020240KA0 K983470 000

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