Clearance Summary
ENURESIS ALARM received FDA 510(k) clearance under submission number K871787, sponsored by Dilorenzo Engineering 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 1987-08-10.
- Submission: K871787
- Applicant / Sponsor: Dilorenzo Engineering Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.2040
- Decision date: 1987-08-10
Classification & Regulation
This clearance is catalogued under FDA product code KPN and 21 CFR 876.2040, within the Gastroenterology, Urology review panel as a Class II device.