ReliefBand— 510(k) K182960

Substantially Equivalent

Reliefband Technologies, LLC

FDA 510(k) clearance K182960 for ReliefBand, Substantially Equivalent on 2019-06-21. Applicant: Reliefband Technologies, LLC. Device class: 2.

Clearance details

Applicant: Reliefband Technologies, LLC
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2018-10-25
Decision date: 2019-06-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Horsham, PA, 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.