Clearance Summary
4 SURE UROLOGICAL CATHETER received FDA 510(k) clearance under submission number K896725, sponsored by The Boston & Pacific Co., Inc.. 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 1990-02-16.
- Submission: K896725
- Applicant / Sponsor: The Boston & Pacific Co., Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5130
- Decision date: 1990-02-16
Classification & Regulation
This clearance is catalogued under FDA product code KOD and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.