Clearance Summary
FIBRE INTERSPACED X-RAY GRID received FDA 510(k) clearance under submission number K963893, sponsored by Smit Rontgen. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1996-11-07.
- Submission: K963893
- Applicant / Sponsor: Smit Rontgen
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1910
- Decision date: 1996-11-07
Classification & Regulation
This clearance is catalogued under FDA product code IXJ and 21 CFR 892.1910, within the Radiology review panel as a Class I device.