RelieVRx— 510(k) K243417

Substantially Equivalent

Appliedvr

FDA 510(k) clearance K243417 for RelieVRx, Substantially Equivalent on 2024-12-04. Applicant: Appliedvr. Device class: 2.

Clearance details

Applicant: Appliedvr
Product code: Code QRA
Device class: Class 2
Regulation: 21 CFR 890.5800
Advisory panel: Neurology
Date received: 2024-11-04
Decision date: 2024-12-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Van Nuys, 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.