VITRABOND LIGHT CURE GLASS IONOMER LINER— 510(k) K882821

Name: FDA 510(k) clearance K882821
Creator: U.S. Food and Drug Administration
Published: 1988-09-15

Substantially Equivalent

3M Company

FDA 510(k) clearance K882821 for VITRABOND LIGHT CURE GLASS IONOMER LINER, Substantially Equivalent on 1988-09-15. Applicant: 3M Company. Device class: 1.

Clearance details

Applicant: 3M Company
Product code: Code EKJ
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1988-07-08
Decision date: 1988-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cottae Grove, MN, US

Download summary PDF View on FDA.gov ↗

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