mobileMOSFET Dosimeter
mobileMOSFET Dosimeter is a MOSFET radiation therapy dosimetry system (FDA Class II; FDA product code IYE, Accelerator, Linear, Medical) made by Best Medical Canada, Ltd., cleared under FDA 510(k) K041557 on 25 Jun 2004 and listed in FDA GUDID since 30 Sep 2016 (UDI-DI 07540146000081), 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 | Number07540146000081 | Date30 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK041557 | Date25 Jun 2004 | StatusActive |
Official records
- AccessGUDID record 07540146000081
- FDA 510(k) database K041557
Across registries
- FDA 510(k) K041557 decided 25 Jun 2004 Active
- FDA GUDID UDI-DI 07540146000081 listed 30 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K041557
- Listed FDA GUDID 07540146000081
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- mobileMOSFET
- Generic name
- MOSFET radiation therapy dosimetry system
- Model / reference
- Dosimeter
- Primary DI / UDI-DI
- 07540146000081
- 510(k) Number
- FDA product code
- IYE
- GMDN term
- MOSFET radiation therapy dosimetry system
- Device class
- Class II
- Regulation number
- 892.5050
- GUDID distribution status
- In Commercial Distribution
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