Clearance Summary
THERAVIEW DIGITAL PORTAL IMAGING COMPUTER received FDA 510(k) clearance under submission number K902339, sponsored by S & S Inficon, 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 1990-08-23.
- Submission: K902339
- Applicant / Sponsor: S & S Inficon, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 1990-08-23
Classification & Regulation
This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.