Clearance Summary
BIPRO MODEL SDS-CB200 received FDA 510(k) clearance under submission number K033118, sponsored by Medical Solutions International. 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 2004-06-28.
- Submission: K033118
- Applicant / Sponsor: Medical Solutions International
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 2004-06-28
Classification & Regulation
This clearance is catalogued under FDA product code FIN and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.