PORCELAIN PRIMER— 510(k) K061322

Substantially Equivalent

J. Morita USA, Inc.

FDA 510(k) clearance K061322 for PORCELAIN PRIMER, Substantially Equivalent on 2006-06-02. Applicant: J. Morita USA, Inc.. Device class: 2.

Clearance details

Applicant: J. Morita USA, Inc.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2006-05-11
Decision date: 2006-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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