Clearance Summary
DUAL LUMEN CATHETER received FDA 510(k) clearance under submission number K043581, sponsored by Acmi Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2005-03-03.
- Submission: K043581
- Applicant / Sponsor: Acmi Corporation
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5130
- Decision date: 2005-03-03
Classification & Regulation
This clearance is catalogued under FDA product code EYB and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.