Clearance Summary
UROTRACT I received FDA 510(k) clearance under submission number K955019, sponsored by Dornier Medtech America, Inc.. 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 1995-12-06.
- Submission: K955019
- Applicant / Sponsor: Dornier Medtech America, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.4890
- Decision date: 1995-12-06
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.