JOHNSON & JOHNSON OPAQUE COLOR MODIFI— 510(k) K830491

Name: FDA 510(k) clearance K830491
Creator: U.S. Food and Drug Administration
Published: 1983-03-17

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K830491 for JOHNSON & JOHNSON OPAQUE COLOR MODIFI, Substantially Equivalent on 1983-03-17. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code EBE
Device class: Class 2
Regulation: 21 CFR 872.3300
Advisory panel: Dental
Date received: 1983-02-15
Decision date: 1983-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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