Clearance Summary
TRIEX-1 HOLLOW FIBER DIALYZER received FDA 510(k) clearance under submission number K760781, sponsored by Extracorporeal Medical Specialities, 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 1976-12-06.
- Submission: K760781
- Applicant / Sponsor: Extracorporeal Medical Specialities, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1976-12-06
Classification & Regulation
This clearance is catalogued under FDA product code FJT and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.