Clearance Summary
KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER received FDA 510(k) clearance under submission number K002901, sponsored by The Kendall Company. 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 2001-03-28.
- Submission: K002901
- Applicant / Sponsor: The Kendall Company
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5540
- Decision date: 2001-03-28
Classification & Regulation
This clearance is catalogued under FDA product code MSD and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.