DIAGNODENT PERIO TIP (ACCESSORY)— 510(k) K042394

Name: FDA 510(k) clearance K042394
Creator: U.S. Food and Drug Administration
Published: 2005-08-02

Substantially Equivalent

Kavo America Corporation

FDA 510(k) clearance K042394 for DIAGNODENT PERIO TIP (ACCESSORY), Substantially Equivalent on 2005-08-02. Applicant: Kavo America Corporation. Device class: 2.

Clearance details

Applicant: Kavo America Corporation
Product code: Code NBL
Device class: Class 2
Regulation: 21 CFR 872.1745
Advisory panel: Dental
Date received: 2004-09-02
Decision date: 2005-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

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