iRelieve Microcurrent Pain Relief System— 510(k) K212618

Name: FDA 510(k) clearance K212618
Creator: U.S. Food and Drug Administration
Published: 2022-09-14

Substantially Equivalent

Fast Track Technologies, Inc.

FDA 510(k) clearance K212618 for iRelieve Microcurrent Pain Relief System, Substantially Equivalent on 2022-09-14. Applicant: Fast Track Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Fast Track Technologies, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2021-08-18
Decision date: 2022-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

Download summary PDF View on FDA.gov ↗

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