3M VITREBOND LIGHT CURE GLASS IONOMER/BASE— 510(k) K962065

Name: FDA 510(k) clearance K962065
Creator: U.S. Food and Drug Administration
Published: 1996-07-18

Substantially Equivalent

3M Company

FDA 510(k) clearance K962065 for 3M VITREBOND LIGHT CURE GLASS IONOMER/BASE, Substantially Equivalent on 1996-07-18. Applicant: 3M Company. Device class: 2.

Clearance details

Applicant: 3M Company
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1996-05-28
Decision date: 1996-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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