VALULINE* AMALGAM ALLOY— 510(k) K821971

Name: FDA 510(k) clearance K821971
Creator: U.S. Food and Drug Administration
Published: 1982-07-20

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K821971 for VALULINE* AMALGAM ALLOY, Substantially Equivalent on 1982-07-20. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code EJJ
Device class: Class 2
Regulation: 21 CFR 872.3070
Advisory panel: Dental
Date received: 1982-07-06
Decision date: 1982-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, US

Download summary PDF View on FDA.gov ↗

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