DENTALOS PLUS MONO, DENTALOS PLUS MULTICOLOR— 510(k) K152215

Name: FDA 510(k) clearance K152215
Creator: U.S. Food and Drug Administration
Published: 2016-01-19

Substantially Equivalent

Dentalplus GmbH

FDA 510(k) clearance K152215 for DENTALOS PLUS MONO, DENTALOS PLUS MULTICOLOR, Substantially Equivalent on 2016-01-19. Applicant: Dentalplus GmbH. Device class: 2.

Clearance details

Applicant: Dentalplus GmbH
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 2015-08-07
Decision date: 2016-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Samerberg, DE

Download summary PDF View on FDA.gov ↗

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