DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC— 510(k) K001269

Name: FDA 510(k) clearance K001269
Creator: U.S. Food and Drug Administration
Published: 2000-06-21

Substantially Equivalent

Dentalmatic Technologies, Inc.

FDA 510(k) clearance K001269 for DENTALMATIC TI PROSTHESIS AND DENTALMATIC TI-A PROSTHETIC, Substantially Equivalent on 2000-06-21. Applicant: Dentalmatic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Dentalmatic Technologies, Inc.
Product code: Code EJH
Device class: Class 2
Regulation: 21 CFR 872.3710
Advisory panel: Dental
Date received: 2000-04-20
Decision date: 2000-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St Laurent, Qc, CA

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