FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUPER PORCELAIN STAIN- PURE WHITE

K Number: K983470 · Decision Dec 22, 1998
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
14
Review Days
82

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SUPER PORCELAIN STAIN- PURE WHITE
K Number
K983470
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Noritake Co., Inc.
Date Received
October 1, 1998
Decision Date
December 22, 1998
Product Code
EIH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EIH Powder, Porcelain

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EIH), ordered by most recent decision date.

View all

Other Clearances by Noritake Co., Inc.

K Number Device Name
K111383 ZIRPRIME
K111107 SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE
K052304 SUPER PORCELAIN EX-3 PRESS
K050920 CZR PRESS LF STAINS
K050160 KATANA ZIRCONIA
K043462 CZR PRESS LF
K031968 CERABIEN ZR
K033049 CZR PRESS
K992023 GRAND CERAM
K992024 SUPER PORCELAIN TI-22
Search all 14 clearances from Noritake Co., Inc. →