MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETH— 510(k) K120404

Name: FDA 510(k) clearance K120404
Creator: U.S. Food and Drug Administration
Published: 2012-05-21

Substantially Equivalent

Merz Dental GmbH

FDA 510(k) clearance K120404 for MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETH, Substantially Equivalent on 2012-05-21. Applicant: Merz Dental GmbH. Device class: 2.

Clearance details

Applicant: Merz Dental GmbH
Product code: Code ELM
Device class: Class 2
Regulation: 21 CFR 872.3590
Advisory panel: Dental
Date received: 2012-02-09
Decision date: 2012-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albuquerque, NM, US

Download summary PDF View on FDA.gov ↗

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