Corvus 09 210295
by Best Nomos
Corvus 09 210295 is a Class II device made by Best Nomos, cleared under FDA 510(k) K100092 on 23 Feb 2010 and listed in FDA GUDID since 23 Aug 2018 (UDI-DI 00852656007427), 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 | Number00852656007427 | Date23 Aug 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK100092 | Date23 Feb 2010 | StatusActive |
Official records
- AccessGUDID record 00852656007427
- FDA 510(k) database K100092
Across registries
- FDA 510(k) K100092 decided 23 Feb 2010 Active
- FDA GUDID UDI-DI 00852656007427 listed 23 Aug 2018 Listed
Timeline
- Cleared FDA 510(k) K100092
- Listed FDA GUDID 00852656007427
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Corvus 09
- Generic name
- Radiation therapy software
- Model / reference
- 210295
- Primary DI / UDI-DI
- 00852656007427
- 510(k) Number
- FDA product code
- MUJ
- GMDN term
- Radiation therapy software
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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