Clearance Summary
SERIES V-SCAN RADIOGRAPHIC FILM SCANNER received FDA 510(k) clearance under submission number K925664, sponsored by Vision Ten, 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 1993-06-22.
- Submission: K925664
- Applicant / Sponsor: Vision Ten, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 1993-06-22
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.