MindMotionPRO— 510(k) K162748

Substantially Equivalent

Mindmaze SA

FDA 510(k) clearance K162748 for MindMotionPRO, Substantially Equivalent on 2017-04-24. 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: 2016-09-30
Decision date: 2017-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lausanne, CH

Download summary PDF View on FDA.gov ↗

Recent devices under product code LXJ

K192474 — VERA2019-10-10
K182333 — Vera2019-04-09
K180880 — DARI Health2019-03-07
K171547 — Qualisys Clinical System2018-08-02
K173931 — MindMotion(TM) GO2018-05-17

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