IN EXAM INTRAORAL DENTAL X-RAY SYSTEM— 510(k) K050019

Name: FDA 510(k) clearance K050019
Creator: U.S. Food and Drug Administration
Published: 2005-01-31

Substantially Equivalent

Kavo America

FDA 510(k) clearance K050019 for IN EXAM INTRAORAL DENTAL X-RAY SYSTEM, Substantially Equivalent on 2005-01-31. Applicant: Kavo America. Device class: 2.

Clearance details

Applicant: Kavo America
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2005-01-05
Decision date: 2005-01-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Zurich, IL, US

Download summary PDF View on FDA.gov ↗

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K252909 — Diagnostic X-Ray Equipment Model POCT222026-02-03

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K051909 — DIAGNODENT2005-10-21
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Data sourced from openFDA. This site is unofficial and independent of the FDA.