Clearance Summary
KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE received FDA 510(k) clearance under submission number K880850, sponsored by Kmb Medical Products 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 1988-05-26.
- Submission: K880850
- Applicant / Sponsor: Kmb Medical Products Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5980
- Decision date: 1988-05-26
Classification & Regulation
This clearance is catalogued under FDA product code FEG and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.