Clearance Summary
MICROFUSE DUAL RATE INFUSER received FDA 510(k) clearance under submission number K091386, sponsored by Numia Medical Technology, LLC. 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 2009-10-02.
- Submission: K091386
- Applicant / Sponsor: Numia Medical Technology, LLC
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 2009-10-02
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.