Clearance Summary
Added Screen Displays For FDA Cleared HeartSee Cardiac P.E.T Processing Software K143664 received FDA 510(k) clearance under submission number K171303, sponsored by University of Texas Medical School AT Houston, Texas. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-09-22.
- Submission: K171303
- Applicant / Sponsor: University of Texas Medical School AT Houston, Texas
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1200
- Decision date: 2017-09-22
Classification & Regulation
This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.