ARTIFICIAL TEETH (ACRYLIC TEETH)— 510(k) K992854

Name: FDA 510(k) clearance K992854
Creator: U.S. Food and Drug Administration
Published: 2000-02-07

Substantially Equivalent

Masterdent Ltda.

FDA 510(k) clearance K992854 for ARTIFICIAL TEETH (ACRYLIC TEETH), Substantially Equivalent on 2000-02-07. Applicant: Masterdent Ltda.. Device class: 2.

Clearance details

Applicant: Masterdent Ltda.
Product code: Code ELM
Device class: Class 2
Regulation: 21 CFR 872.3590
Advisory panel: Dental
Date received: 1999-08-24
Decision date: 2000-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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K122852 — PHYSIOSTAR NFC2012-12-06
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Data sourced from openFDA. This site is unofficial and independent of the FDA.