TrueRelief Device— 510(k) K202186

Substantially Equivalent

Truerelief

FDA 510(k) clearance K202186 for TrueRelief Device, Substantially Equivalent on 2021-03-23. Applicant: Truerelief. Device class: 2.

Clearance details

Applicant: Truerelief
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2020-08-04
Decision date: 2021-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, 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.