Clearance Summary
BAXJECT II HI-FLOW NEEDLELESS TRANSFER DEVICE received FDA 510(k) clearance under submission number K092318, sponsored by Baxter Healthcare Corporation. 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 2009-10-30.
- Submission: K092318
- Applicant / Sponsor: Baxter Healthcare Corporation
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5440
- Decision date: 2009-10-30
Classification & Regulation
This clearance is catalogued under FDA product code LHI and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.