DURODENT CORPORATION ARTIFICIAL PLASTIC TEETH— 510(k) K933737

Name: FDA 510(k) clearance K933737
Creator: U.S. Food and Drug Administration
Published: 1994-06-13

Substantially Equivalent

Durodent Corp.

FDA 510(k) clearance K933737 for DURODENT CORPORATION ARTIFICIAL PLASTIC TEETH, Substantially Equivalent on 1994-06-13. Applicant: Durodent Corp.. Device class: 2.

Clearance details

Applicant: Durodent Corp.
Product code: Code ELM
Device class: Class 2
Regulation: 21 CFR 872.3590
Advisory panel: Dental
Date received: 1993-08-02
Decision date: 1994-06-13
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
K121749 — VERACIA2012-09-07

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