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

PALFIQUE LIGHT LINER

K Number: K896980 · Decision May 15, 1990
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
22
Review Days
153

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Basic Information

Device Name
PALFIQUE LIGHT LINER
K Number
K896980
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Tokuyama America, Inc.
Date Received
December 13, 1989
Decision Date
May 15, 1990
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

Similar 510(k) Clearances

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Other Clearances by Tokuyama America, Inc.

K Number Device Name
K022641 TOKUYAMA REBASE II
K011854 TOKUYAMA M-BOND
K011685 BISTITE II DC
K010267 PALFIQUE ESTELITE LV CLEAR
K002863 PALFIQUE ESTELITE LV
K993917 TOKUYAMA ONE-UP-BOND F
K991711 BISTITE II SC
K982537 TOKUYAMA SOFRELINER
K980054 PALFIQUE ESTELITE
K980058 TOKUSO MAC BOND II
Search all 22 clearances from Tokuyama America, Inc. →