Clearance Summary
Sapphire Infusion Pump, Sapphire administration sets received FDA 510(k) clearance under submission number K192860, sponsored by Q Core Medical , Ltd.. 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 2020-11-19.
- Submission: K192860
- Applicant / Sponsor: Q Core Medical , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 2020-11-19
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.