Clearance Summary
VESISCAN received FDA 510(k) clearance under submission number K093485, sponsored by Life-Tech, 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 2010-03-16.
- Submission: K093485
- Applicant / Sponsor: Life-Tech, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2010-03-16
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.