Clearance Summary
TM-CAPD received FDA 510(k) clearance under submission number K812615, sponsored by Tri-Med, 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 1982-01-05.
- Submission: K812615
- Applicant / Sponsor: Tri-Med, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5630
- Decision date: 1982-01-05
Classification & Regulation
This clearance is catalogued under FDA product code KPP and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.