BRIGHTGLASS BRIGHTGLASS M— 510(k) K122025

Name: FDA 510(k) clearance K122025
Creator: U.S. Food and Drug Administration
Published: 2012-10-09

Substantially Equivalent

Ktk Medical Supplies GmbH

FDA 510(k) clearance K122025 for BRIGHTGLASS BRIGHTGLASS M, Substantially Equivalent on 2012-10-09. Applicant: Ktk Medical Supplies GmbH. Device class: 2.

Clearance details

Applicant: Ktk Medical Supplies GmbH
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 2012-07-11
Decision date: 2012-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Germering, DE

Download summary PDF View on FDA.gov ↗

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