Clearance Summary
CORFLO ANTI-IV ENTERAL FEEDING EXTENSION SET, MODELS 20-1006AIV-LB AND 20-1030AIV-LB received FDA 510(k) clearance under submission number K083786, sponsored by Corpak Medsystems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2009-02-20.
- Submission: K083786
- Applicant / Sponsor: Corpak Medsystems
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5980
- Decision date: 2009-02-20
Classification & Regulation
This clearance is catalogued under FDA product code FPD and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.