K251519
- 510(k) number
- K251519
- Device name
- RelieVRx (Pico G3)
- Applicant
- Appliedvr CA · US
- Product code
- QRA — Virtual Reality Behavioral Therapy Device For Pain R
- Decision date
- 2025-08-13
- Date received
- 2025-05-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251519.pdf
Official FDA record: K251519
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.