NON-EUGENOL TEMPORARY CEMENT— 510(k) K020158

Name: FDA 510(k) clearance K020158
Creator: U.S. Food and Drug Administration
Published: 2002-03-07

Substantially Equivalent

J. Morita USA, Inc.

FDA 510(k) clearance K020158 for NON-EUGENOL TEMPORARY CEMENT, Substantially Equivalent on 2002-03-07. Applicant: J. Morita USA, Inc.. Device class: 1.

Clearance details

Applicant: J. Morita USA, Inc.
Product code: Code EMB
Device class: Class 1
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2002-01-17
Decision date: 2002-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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