INTERLIG— 510(k) K123823

Name: FDA 510(k) clearance K123823
Creator: U.S. Food and Drug Administration
Published: 2013-05-31

Substantially Equivalent

Angelus Industria DE Productos Odontologicos

FDA 510(k) clearance K123823 for INTERLIG, Substantially Equivalent on 2013-05-31. Applicant: Angelus Industria DE Productos Odontologicos. Device class: 2.

Clearance details

Applicant: Angelus Industria DE Productos Odontologicos
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2012-12-12
Decision date: 2013-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aventura, FL, US

Download summary PDF View on FDA.gov ↗

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