Clearance Summary
GENESIS REUSABLE RIGID CONTAINER SYSTEM received FDA 510(k) clearance under submission number K140850, sponsored by Carefusion 2200, 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 2014-08-27.
- Submission: K140850
- Applicant / Sponsor: Carefusion 2200, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6850
- Decision date: 2014-08-27
Classification & Regulation
This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.