Clearance Summary
RAREX & OPTEX X-RAY SCREENS received FDA 510(k) clearance under submission number K902039, sponsored by Mci Optonix, 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 1990-07-27.
- Submission: K902039
- Applicant / Sponsor: Mci Optonix, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.1960
- Decision date: 1990-07-27
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.