Clearance Summary
GammaBeam 500 received FDA 510(k) clearance under submission number K150191, sponsored by Best Theratronics Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2015-04-17.
- Submission: K150191
- Applicant / Sponsor: Best Theratronics Limited
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5750
- Decision date: 2015-04-17
Classification & Regulation
This clearance is catalogued under FDA product code IWB and 21 CFR 892.5750, within the Radiology review panel as a Class II device.