DEXIS CariVu 3-in-1 by KaVo— 510(k) K182712

Name: FDA 510(k) clearance K182712
Creator: U.S. Food and Drug Administration
Published: 2019-11-23

Substantially Equivalent

Kaltenbach & Voigt GmbH

FDA 510(k) clearance K182712 for DEXIS CariVu 3-in-1 by KaVo, Substantially Equivalent on 2019-11-23. Applicant: Kaltenbach & Voigt GmbH. Device class: 2.

Clearance details

Applicant: Kaltenbach & Voigt GmbH
Product code: Code NTK
Device class: Class 2
Regulation: 21 CFR 872.1745
Advisory panel: Dental
Date received: 2018-09-27
Decision date: 2019-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Biberach, DE

Download summary PDF View on FDA.gov ↗

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