Clearance Summary
SYN-OPTICS #5200 received FDA 510(k) clearance under submission number K820624, sponsored by Syn-Optics. 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: K820624
- Applicant / Sponsor: Syn-Optics
- 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 FET and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.