Clearance Summary
INSTATRAK 3000 SYSTEM WITH FLUOROTRAK MODULE, MODEL IT3000 received FDA 510(k) clearance under submission number K994270, sponsored by Visualization Technology, 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 2000-03-09.
- Submission: K994270
- Applicant / Sponsor: Visualization Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2000-03-09
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.