Clearance Summary
SUPRAPUBIC CATHETER AND INTRODUCER SET received FDA 510(k) clearance under submission number K132890, sponsored by Mediplus , Ltd.. 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 2014-01-17.
- Submission: K132890
- Applicant / Sponsor: Mediplus , Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5090
- Decision date: 2014-01-17
Classification & Regulation
This clearance is catalogued under FDA product code KOB and 21 CFR 876.5090, within the Gastroenterology, Urology review panel as a Class II device.