Mobius3D 2.2
by Varian Medical Systems, Inc.
Mobius3D 2.2 is a Class II device made by Varian Medical Systems, Inc., cleared under FDA 510(k) K191761 on 31 Jul 2019 and listed in FDA GUDID since 5 Jun 2020 (UDI-DI 00899475002462), active as of 8 Nov 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00899475002462 | Date5 Jun 2020 | StatusListed |
| United States | FDA 510(k) | NumberK191761 | Date31 Jul 2019 | StatusActive |
Official records
- AccessGUDID record 00899475002462
- FDA 510(k) database K191761
Across registries
- FDA 510(k) K191761 decided 31 Jul 2019 Active
- FDA GUDID UDI-DI 00899475002462 listed 5 Jun 2020 Listed
Timeline
- Cleared FDA 510(k) K191761
- Listed FDA GUDID 00899475002462
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mobius3D
- Generic name
- Radiation therapy software
- Model / reference
- 2.2
- Primary DI / UDI-DI
- 00899475002462
- 510(k) Number
- FDA product code
- IYE
- GMDN term
- Radiation therapy software
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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