Clearance Summary
FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3 received FDA 510(k) clearance under submission number K820790, sponsored by American Optical Corp.. 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 1982-04-01.
- Submission: K820790
- Applicant / Sponsor: American Optical Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1982-04-01
Classification & Regulation
This clearance is catalogued under FDA product code FAM and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.