Clearance Summary
MAHURKAR TRIPLE LUMEN CATHETER, 12 FR received FDA 510(k) clearance under submission number K020089, 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 2002-04-10.
- Submission: K020089
- Applicant / Sponsor: The Kendall Company
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5540
- Decision date: 2002-04-10
Classification & Regulation
This clearance is catalogued under FDA product code NIE and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.