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mobileMOSFET Dosimeter

by Best Medical Canada, Ltd.

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 United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K041557

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07540146000081 UDI-DI Date30 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK041557 Date25 Jun 2004DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K041557 decided 25 Jun 2004 Active
  • FDA GUDID UDI-DI 07540146000081 listed 30 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K041557
  2. Listed FDA GUDID 07540146000081

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

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

Similar devices

Other devices filed under FDA product code IYE (Accelerator, Linear, Medical).

Other devices from Best Medical Canada, Ltd.

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)