FUSION SINGLE LINK— 510(k) K132923

Name: FDA 510(k) clearance K132923
Creator: U.S. Food and Drug Administration
Published: 2014-01-03

Substantially Equivalent

Angelus Industria DE Productos Odontologicos SA

FDA 510(k) clearance K132923 for FUSION SINGLE LINK, Substantially Equivalent on 2014-01-03. Applicant: Angelus Industria DE Productos Odontologicos SA. Device class: 2.

Clearance details

Applicant: Angelus Industria DE Productos Odontologicos SA
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2013-09-18
Decision date: 2014-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aventura, FL, US

Download summary PDF View on FDA.gov ↗

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