Clearance Summary
BETA 90/50 MOBILE IMAGING TABLE received FDA 510(k) clearance under submission number K884531, sponsored by Beta Medical Products Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1989-01-11.
- Submission: K884531
- Applicant / Sponsor: Beta Medical Products Co.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1980
- Decision date: 1989-01-11
Classification & Regulation
This clearance is catalogued under FDA product code IXR and 21 CFR 892.1980, within the Radiology review panel as a Class II device.