Clearance Summary
RECTAL TUBE DEVICE received FDA 510(k) clearance under submission number K760886, sponsored by Van Sickle Plastics 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 1976-12-09.
- Submission: K760886
- Applicant / Sponsor: Van Sickle Plastics Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5900
- Decision date: 1976-12-09
Classification & Regulation
This clearance is catalogued under FDA product code EXB and 21 CFR 876.5900, within the Gastroenterology, Urology review panel as a Class I device.