Clearance Summary
HORIZONTAL RADIOGRAPHIC 4/WAY FLOATING received FDA 510(k) clearance under submission number K792169, sponsored by Bennett X-Ray 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 1979-12-10.
- Submission: K792169
- Applicant / Sponsor: Bennett X-Ray Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1980
- Decision date: 1979-12-10
Classification & Regulation
This clearance is catalogued under FDA product code IZZ and 21 CFR 892.1980, within the Radiology review panel as a Class II device.