ULab Systems Treatment Planning Software— 510(k) K171295

Name: FDA 510(k) clearance K171295
Creator: U.S. Food and Drug Administration
Published: 2018-01-09

Substantially Equivalent

Ulab Systems, Inc.

FDA 510(k) clearance K171295 for ULab Systems Treatment Planning Software, Substantially Equivalent on 2018-01-09. Applicant: Ulab Systems, Inc.. Device class: 2.

Clearance details

Applicant: Ulab Systems, Inc.
Product code: Code PNN
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2017-05-02
Decision date: 2018-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, 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.