MindMotion(TM) GO— 510(k) K173931

Substantially Equivalent

Mindmaze SA

FDA 510(k) clearance K173931 for MindMotion(TM) GO, Substantially Equivalent on 2018-05-17. Applicant: Mindmaze SA. Device class: 2.

Clearance details

Applicant: Mindmaze SA
Product code: Code LXJ
Device class: Class 2
Regulation: 21 CFR 890.5360
Advisory panel: Physical Medicine
Date received: 2017-12-26
Decision date: 2018-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lausanne, CH

Download summary PDF View on FDA.gov ↗

Recent devices under product code LXJ

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K182333 — Vera2019-04-09
K180880 — DARI Health2019-03-07
K171547 — Qualisys Clinical System2018-08-02
K172882 — UINCARE HOME2018-05-10

More clearances from Mindmaze SA

K162748 — MindMotionPRO2017-04-24

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