CZR PRESS

Powder, Porcelain

NORITAKE CO., INC.

The following data is part of a premarket notification filed by Noritake Co., Inc. with the FDA for Czr Press.

Pre-market Notification Details

• Device ID: K033049
• 510k Number: K033049
• Device Name: CZR PRESS
• Classification: Powder, Porcelain
• Applicant: NORITAKE CO., INC. 3050 K STREET, NW, STE 400 Washington, DC 20007
• Contact: Ivan J Wasserman
• Correspondent: Ivan J Wasserman; NORITAKE CO., INC. 3050 K STREET, NW, STE 400 Washington, DC 20007
• Product Code: EIH
• CFR Regulation Number: 872.6660 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2003-09-29
• Decision Date: 2003-10-24

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
EKUR1070721KA0	K033049	000
EKUR1070661KA0	K033049	000
EKUR1070652KA0	K033049	000
EKUR1070651KA0	K033049	000
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EKUR1070671KA0	K033049	000
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EKUR1070711KA0	K033049	000
EKUR1070702KA0	K033049	000
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EKUR1070692KA0	K033049	000
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EKUR1070612KA0	K033049	000
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EKUR1070602KA0	K033049	000
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EKUR1070541KA0	K033049	000
EKUR1070532KA0	K033049	000
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EKUR1070522KA0	K033049	000
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EKUR1070511KA0	K033049	000
EKUR1070040KA0	K033049	000
EKUR1070551KA0	K033049	000
EKUR1070552KA0	K033049	000
EKUR1070601KA0	K033049	000
EKUR1070592KA0	K033049	000
EKUR1070591KA0	K033049	000
EKUR1070582KA0	K033049	000
EKUR1070581KA0	K033049	000
EKUR1070572KA0	K033049	000
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