Varian Verification Console 2.3
by Varian Medical Systems India Software Private Limited
Varian Verification Console 2.3 is a Class II device made by Varian Medical Systems India Software Private Limited, cleared under FDA 510(k) K124002 on 21 Feb 2013 and listed in FDA GUDID since 8 Nov 2019 (UDI-DI 00856104006123), active as of 22 Oct 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 | Number00856104006123 | Date8 Nov 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK124002 | Date21 Feb 2013 | StatusActive |
Official records
- AccessGUDID record 00856104006123
- FDA 510(k) database K124002
Across registries
- FDA 510(k) K124002 decided 21 Feb 2013 Active
- FDA GUDID UDI-DI 00856104006123 listed 8 Nov 2019 Listed
Timeline
- Cleared FDA 510(k) K124002
- Listed FDA GUDID 00856104006123
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Varian Verification Console
- Generic name
- Radiation therapy treatment record/verify system
- Model / reference
- 2.3
- Primary DI / UDI-DI
- 00856104006123
- 510(k) Number
- FDA product code
- LHN
- GMDN term
- Radiation therapy treatment record/verify system
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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