Clearance Summary
MODIFIED PORGES SPEC 5* SUPRAPUBIC CATHETER received FDA 510(k) clearance under submission number K901603, sponsored by Bivona Medical Technologies. 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 1990-05-04.
- Submission: K901603
- Applicant / Sponsor: Bivona Medical Technologies
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5090
- Decision date: 1990-05-04
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.