Clearance Summary
LINEAR ACCELERATOR THERAC 25 received FDA 510(k) clearance under submission number K837347, sponsored by Atomic Energy of Canada. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1983-06-24.
- Submission: K837347
- Applicant / Sponsor: Atomic Energy of Canada
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 1983-06-24
Classification & Regulation
This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.