RelieVRx RVX-3021
by Appliedvr United States GUDID
Product code QRA
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850038247126 | Date16 Jan 2025 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- RelieVRx
- Generic Name
- Pain relief virtual reality system
- Model / Reference
- RVX-3021
- Primary DI / UDI-DI
- 00850038247126
- 510(k) Number
- FDA Product Code
- QRA
- GMDN Term
- Pain relief virtual reality system
- Device Class
- Class II
- Regulation Number
- 890.5800
- Commercial Distribution
- In Commercial Distribution
Other devices from Appliedvr
Properties & raw data
Show properties, registry sources and raw records
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 6717a276-c3b3-42cd-871a-54bc5cbdc08f