Clearance Summary
DIGORA received FDA 510(k) clearance under submission number K934949, sponsored by Orion Corporation Soredex. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-02-10.
- Submission: K934949
- Applicant / Sponsor: Orion Corporation Soredex
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1630
- Decision date: 1994-02-10
Classification & Regulation
This clearance is catalogued under FDA product code IXK and 21 CFR 892.1630, within the Radiology review panel as a Class II device.