Clearance Summary
PARAGON INFUSION SYSTEM received FDA 510(k) clearance under submission number K020251, sponsored by I-Flow Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2002-02-15.
- Submission: K020251
- Applicant / Sponsor: I-Flow Corp.
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 2002-02-15
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.