Clearance Summary
INFUSET W/HUBER NEEDLE received FDA 510(k) clearance under submission number K844313, sponsored by Med Fusion Systems, 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 1985-01-22.
- Submission: K844313
- Applicant / Sponsor: Med Fusion Systems, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 1985-01-22
Classification & Regulation
This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.