EaseVRx— 510(k) DEN210014

Unknown

Appliedvr, Inc.

FDA 510(k) clearance DEN210014 for EaseVRx, Unknown on 2021-11-16. Applicant: Appliedvr, Inc.. Device class: 2.

Clearance details

Applicant: Appliedvr, Inc.
Product code: Code QRA
Device class: Class 2
Regulation: 21 CFR 890.5800
Advisory panel: Neurology
Date received: 2021-03-30
Decision date: 2021-11-16
Decision: Unknown
Clearance type: Direct
Location: Van Nuys, CA, US

View on FDA.gov ↗

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