Clearance Summary
THE KENDALL URINARY OUTPUT MONITOR received FDA 510(k) clearance under submission number K852083, sponsored by The Kendal Co.. 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 1985-09-20.
- Submission: K852083
- Applicant / Sponsor: The Kendal Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.4730
- Decision date: 1985-09-20
Classification & Regulation
This clearance is catalogued under FDA product code FFO and 21 CFR 876.4730, within the Gastroenterology, Urology review panel as a Class I device.