Clearance Summary
ULTRA-VISION SUPER RAPID INTENSIFYING SCREEN received FDA 510(k) clearance under submission number K933161, sponsored by Dupont Medical Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1993-10-07.
- Submission: K933161
- Applicant / Sponsor: Dupont Medical Products
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1960
- Decision date: 1993-10-07
Classification & Regulation
This clearance is catalogued under FDA product code EAM and 21 CFR 892.1960, within the Radiology review panel as a Class I device.