GULLIVER AND CLASSE A— 510(k) K012213

Name: FDA 510(k) clearance K012213
Creator: U.S. Food and Drug Administration
Published: 2001-08-13

Substantially Equivalent

American Dental Technologies, Inc.

FDA 510(k) clearance K012213 for GULLIVER AND CLASSE A, Substantially Equivalent on 2001-08-13. Applicant: American Dental Technologies, Inc.. Device class: 1.

Clearance details

Applicant: American Dental Technologies, Inc.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2001-07-16
Decision date: 2001-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Corpus Christi, TX, US

Download summary PDF View on FDA.gov ↗

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