MyndMove 2.0— 510(k) K212149

Substantially Equivalent

Myndtec, Inc.

FDA 510(k) clearance K212149 for MyndMove 2.0, Substantially Equivalent on 2022-03-03. Applicant: Myndtec, Inc.. Device class: 2.

Clearance details

Applicant: Myndtec, Inc.
Product code: Code GZI
Device class: Class 2
Regulation: 21 CFR 882.5810
Advisory panel: Neurology
Date received: 2021-07-09
Decision date: 2022-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, CA

Download summary PDF View on FDA.gov ↗

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