K243417
- 510(k) number
- K243417
- Device name
- RelieVRx
- Applicant
- Appliedvr CA · US
- Product code
- QRA — Virtual Reality Behavioral Therapy Device For Pain R
- Decision date
- 2024-12-04
- Date received
- 2024-11-04
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K243417.pdf
Official FDA record: K243417
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.