Clearance Summary
PennPET Explorer Positron Emission Tomograph received FDA 510(k) clearance under submission number K251401, sponsored by Trustees of the University of Pennsylvania. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-11-25.
- Submission: K251401
- Applicant / Sponsor: Trustees of the University of Pennsylvania
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1200
- Decision date: 2025-11-25
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.