Clearance Summary
CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND received FDA 510(k) clearance under submission number K862734, sponsored by D&R X-Ray Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1986-08-01.
- Submission: K862734
- Applicant / Sponsor: D&R X-Ray Products, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1770
- Decision date: 1986-08-01
Classification & Regulation
This clearance is catalogued under FDA product code IYB and 21 CFR 892.1770, within the Radiology review panel as a Class I device.