Clearance Summary
MRX-280 received FDA 510(k) clearance under submission number K942040, sponsored by Mrx 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 1994-07-05.
- Submission: K942040
- Applicant / Sponsor: Mrx Corp.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1750
- Decision date: 1994-07-05
Classification & Regulation
This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.