Clearance Summary
MEDRAD® Imaging Bulk Package Transfer Spike received FDA 510(k) clearance under submission number K253688, sponsored by Bayer Medical Care, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2026-06-12.
- Submission: K253688
- Applicant / Sponsor: Bayer Medical Care, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 2026-06-12
Classification & Regulation
This clearance is catalogued under FDA product code PQH and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.