Dosimetry Check 5
Dosimetry Check 5 is a Class II device made by Math Resolutions, LLC, cleared under FDA 510(k) K162577 on 18 Nov 2016 (3 earlier submissions) and listed in FDA GUDID since 8 Dec 2016 (UDI-DI B229DC051), active as of 23 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 | NumberB229DC051 | Date8 Dec 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK162577 | Date18 Nov 2016 | StatusActive |
Official records
- FDA 510(k) database K162577
- FDA 510(k) database K132605
- FDA 510(k) database K101503
- FDA 510(k) database K010225
Across registries
- FDA 510(k) K162577 decided 18 Nov 2016 Active
- FDA GUDID UDI-DI B229DC051 listed 8 Dec 2016 Listed
Timeline
- Cleared FDA 510(k) K010225
- Cleared FDA 510(k) K101503
- Cleared FDA 510(k) K132605
- Cleared FDA 510(k) K162577
- Listed FDA GUDID B229DC051
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Dosimetry Check
- Generic name
- Radiation therapy software
- Model / reference
- 5
- Primary DI / UDI-DI
- B229DC051
- 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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