FUTURABOND M/FUTURABOND M SINGLE DOSE— 510(k) K082753

Name: FDA 510(k) clearance K082753
Creator: U.S. Food and Drug Administration
Published: 2008-11-24

Substantially Equivalent

Voco GmbH

FDA 510(k) clearance K082753 for FUTURABOND M/FUTURABOND M SINGLE DOSE, Substantially Equivalent on 2008-11-24. Applicant: Voco GmbH. Device class: 2.

Clearance details

Applicant: Voco GmbH
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2008-09-19
Decision date: 2008-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cuxhaven, DE

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.