Verification Console 2.1
by Varian Medical Systems India Software Private Limited
Verification Console 2.1 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 16 Sep 2016 (UDI-DI 00856104006024), 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 | Number00856104006024 | Date16 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK124002 | Date21 Feb 2013 | StatusActive |
Official records
- AccessGUDID record 00856104006024
- FDA 510(k) database K124002
Across registries
- FDA 510(k) K124002 decided 21 Feb 2013 Active
- FDA GUDID UDI-DI 00856104006024 listed 16 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K124002
- Listed FDA GUDID 00856104006024
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Verification Console
- Generic name
- Radiation therapy treatment record/verify system
- Model / reference
- 2.1
- Primary DI / UDI-DI
- 00856104006024
- 510(k) Number
- FDA product code
- IYE
- 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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