Clearance Summary
THE OMNI-FLOW THERAPIST INFUSION MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K882594, sponsored by Omni-Flow, 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 1988-09-20.
- Submission: K882594
- Applicant / Sponsor: Omni-Flow, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 1988-09-20
Classification & Regulation
This clearance is catalogued under FDA product code FRN and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.