Clearance Summary
CRISA received FDA 510(k) clearance under submission number K833847, sponsored by X-Ray Tube Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1983-12-12.
- Submission: K833847
- Applicant / Sponsor: X-Ray Tube Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1760
- Decision date: 1983-12-12
Classification & Regulation
This clearance is catalogued under FDA product code ITY and 21 CFR 892.1760, within the Radiology review panel as a Class I device.