CLEARFIL CERAMIC PRIMER PLUS, CLEARFIL CERAMIC PRIMER PLUS (Trial)— 510(k) K150703

Name: FDA 510(k) clearance K150703
Creator: U.S. Food and Drug Administration
Published: 2015-08-13

Substantially Equivalent

Kuraray Noritake Dental, Inc.

FDA 510(k) clearance K150703 for CLEARFIL CERAMIC PRIMER PLUS, CLEARFIL CERAMIC PRIMER PLUS (Trial), Substantially Equivalent on 2015-08-13. Applicant: Kuraray Noritake Dental, Inc.. Device class: 2.

Clearance details

Applicant: Kuraray Noritake Dental, Inc.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2015-03-18
Decision date: 2015-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chiyoda-Ku, JP

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.