Clearance Summary
UR 150-UR 150T received FDA 510(k) clearance under submission number K801723, sponsored by Siemens 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 1980-08-13.
- Submission: K801723
- Applicant / Sponsor: Siemens Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.4890
- Decision date: 1980-08-13
Classification & Regulation
This clearance is catalogued under FDA product code KQS and 21 CFR 876.4890, within the Gastroenterology, Urology review panel as a Class I device.